CN107793308A - A kind of synthetic method of the methoxy benzoic acid of 2 methyl 3 - Google Patents
A kind of synthetic method of the methoxy benzoic acid of 2 methyl 3 Download PDFInfo
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- CN107793308A CN107793308A CN201610774009.7A CN201610774009A CN107793308A CN 107793308 A CN107793308 A CN 107793308A CN 201610774009 A CN201610774009 A CN 201610774009A CN 107793308 A CN107793308 A CN 107793308A
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- methyl
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- methoxy benzoic
- benzoic acids
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- 238000010189 synthetic method Methods 0.000 title claims abstract description 24
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 title abstract 7
- ZEYHEAKUIGZSGI-UHFFFAOYSA-N 4-methoxybenzoic acid Chemical compound COC1=CC=C(C(O)=O)C=C1 ZEYHEAKUIGZSGI-UHFFFAOYSA-N 0.000 title abstract 4
- ILUJQPXNXACGAN-UHFFFAOYSA-N ortho-methoxybenzoic acid Natural products COC1=CC=CC=C1C(O)=O ILUJQPXNXACGAN-UHFFFAOYSA-N 0.000 title abstract 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 claims abstract description 42
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 claims abstract description 30
- 238000006243 chemical reaction Methods 0.000 claims abstract description 23
- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical compound CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 claims abstract description 15
- 238000009413 insulation Methods 0.000 claims abstract description 12
- RDHPKYGYEGBMSE-UHFFFAOYSA-N bromoethane Chemical compound CCBr RDHPKYGYEGBMSE-UHFFFAOYSA-N 0.000 claims abstract description 9
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000011777 magnesium Substances 0.000 claims abstract description 8
- 229910052749 magnesium Inorganic materials 0.000 claims abstract description 8
- 239000000843 powder Substances 0.000 claims abstract description 8
- 150000003839 salts Chemical class 0.000 claims abstract description 7
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims abstract description 6
- 235000011089 carbon dioxide Nutrition 0.000 claims abstract description 6
- 238000003756 stirring Methods 0.000 claims abstract description 6
- JPCISVSOTKMFPG-UHFFFAOYSA-N 3-methoxy-2-methylbenzoic acid Chemical class COC1=CC=CC(C(O)=O)=C1C JPCISVSOTKMFPG-UHFFFAOYSA-N 0.000 claims description 24
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 16
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 15
- LTVRGAWOEOKGJZ-UHFFFAOYSA-N 1-chloro-3-methoxy-2-methylbenzene Chemical class COC1=CC=CC(Cl)=C1C LTVRGAWOEOKGJZ-UHFFFAOYSA-N 0.000 claims description 14
- 239000000706 filtrate Substances 0.000 claims description 10
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 8
- 239000002253 acid Substances 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 230000006837 decompression Effects 0.000 claims description 5
- 239000012044 organic layer Substances 0.000 claims description 5
- 239000000047 product Substances 0.000 claims description 5
- TXUICONDJPYNPY-UHFFFAOYSA-N (1,10,13-trimethyl-3-oxo-4,5,6,7,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-17-yl) heptanoate Chemical group C1CC2CC(=O)C=C(C)C2(C)C2C1C1CCC(OC(=O)CCCCCC)C1(C)CC2 TXUICONDJPYNPY-UHFFFAOYSA-N 0.000 claims description 4
- 229910021626 Tin(II) chloride Inorganic materials 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 4
- 239000002585 base Substances 0.000 claims description 4
- 239000001119 stannous chloride Substances 0.000 claims description 4
- 235000011150 stannous chloride Nutrition 0.000 claims description 4
- DOBRDRYODQBAMW-UHFFFAOYSA-N copper(i) cyanide Chemical compound [Cu+].N#[C-] DOBRDRYODQBAMW-UHFFFAOYSA-N 0.000 claims description 3
- 238000001704 evaporation Methods 0.000 claims description 2
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 1
- 150000001335 aliphatic alkanes Chemical class 0.000 claims 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 1
- 229910052794 bromium Inorganic materials 0.000 claims 1
- QGRPVMLBTFGQDQ-UHFFFAOYSA-N 1-chloro-2-methoxybenzene Chemical compound COC1=CC=CC=C1Cl QGRPVMLBTFGQDQ-UHFFFAOYSA-N 0.000 abstract description 5
- 238000010438 heat treatment Methods 0.000 abstract description 4
- 239000002994 raw material Substances 0.000 description 6
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical class COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 3
- 238000001035 drying Methods 0.000 description 3
- 230000008030 elimination Effects 0.000 description 3
- 238000003379 elimination reaction Methods 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- YPQAFWHSMWWPLX-UHFFFAOYSA-N 1975-50-4 Chemical class CC1=C(C(O)=O)C=CC=C1[N+]([O-])=O YPQAFWHSMWWPLX-UHFFFAOYSA-N 0.000 description 2
- DTFKRVXLBCAIOZ-UHFFFAOYSA-N 2-methylanisole Chemical compound COC1=CC=CC=C1C DTFKRVXLBCAIOZ-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 239000000543 intermediate Substances 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- XFXPMWWXUTWYJX-UHFFFAOYSA-N Cyanide Chemical compound N#[C-] XFXPMWWXUTWYJX-UHFFFAOYSA-N 0.000 description 1
- 239000005917 Methoxyfenozide Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000003054 catalyst Substances 0.000 description 1
- 239000003610 charcoal Substances 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 description 1
- 150000005573 methoxybenzenes Chemical class 0.000 description 1
- QCAWEPFNJXQPAN-UHFFFAOYSA-N methoxyfenozide Chemical compound COC1=CC=CC(C(=O)NN(C(=O)C=2C=C(C)C=C(C)C=2)C(C)(C)C)=C1C QCAWEPFNJXQPAN-UHFFFAOYSA-N 0.000 description 1
- 238000006198 methoxylation reaction Methods 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 231100000004 severe toxicity Toxicity 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000003053 toxin Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/16—Preparation of ethers by reaction of esters of mineral or organic acids with hydroxy or O-metal groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/15—Preparation of carboxylic acids or their salts, halides or anhydrides by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The present invention relates to a kind of synthetic method of the methoxy benzoic acid of 2 methyl 3, specific steps include：A. appropriate sodium methoxide solution, 2 are added in a kettle, and 6 dichlorotoleune, dimethylformamide and cuprous salt stirring heating, temperature control are reacted at 80 DEG C~150 DEG C, obtain the chloroanisole of 2 methyl 3；B. added appropriate butyl oxide and magnesium in another reactor, temperature control adds the mixed liquor of bromoethane and the chloroanisole of 2 methyl 3 at 30 DEG C~60 DEG C, after reacting 20min~40min, the chloroanisole of 2 methyl 3 is added dropwise at 40 DEG C~60 DEG C in temperature control, rear insulation reaction 1.5h~2.5h is added dropwise, it is subsequently cooled to 15 DEG C~5 DEG C, dry ice is added by batch, temperature control is in 0 DEG C~20 DEG C insulation reaction 2h~4h, then butyl oxide is reclaimed, it is the methoxy benzoic acid of 2 methyl 3 that adjustment ph values, which separate out white powder,.The synthetic method route of the methoxy benzoic acid of 2 methyl 3 of the present invention is succinct and yield is high.
Description
Technical field
The present invention relates to a kind of synthetic method of compound, especially a kind of synthesis of 2- methyl -3- methoxy benzoic acids
Method.
Background technology
2- methyl -3- methoxy benzoic acids are organic synthesis intermediates important in agricultural chemicals, medical industry, especially efficiently
The important intermediate of low-toxin farm chemicals methoxyfenozide.The synthetic method of 2- methyl -3- methoxy benzoic acids have it is a variety of, wherein applying
Relatively broad one kind is using 3- nitro -2- methyl benzoic acids as raw material, through reduction, diazotising, methoxylation, obtains 2- first
Base -3- methoxy benzoic acids.But using 3- nitro -2- methyl benzoic acids as raw material, the raw material sources are difficult, price, industry
It is melted into this height.Another method is using 2,6-DCT as raw material, and etherified, cyaniding, hydrolysis obtain 2- methyl -3- methoxies
Yl benzoic acid.Because the cyanide using severe toxicity is as catalyst, more problem be present, and there are the more three wastes, therefore also not
Suitable industrialized production.
How to provide a kind of synthetic method for the 2- methyl -3- methoxy benzoic acids that route is succinct and yield is high is this area
Technical staff's technical issues that need to address.
The content of the invention
2- methyl -3- methoxybenzene the first succinct and high yield the technical problem to be solved in the present invention is to provide a kind of route
The synthetic method of acid.
The present invention is to solve a kind of technical scheme that above-mentioned technical problem proposes to be：A kind of 2- methyl -3- methoxybenzene first
The synthetic method of acid, specific steps include：
A. appropriate sodium methoxide solution, 2,6- dichlorotoleune, dimethylformamide and cuprous salt stirring is added in a kettle to rise
Temperature, temperature control are reacted at 80 DEG C~150 DEG C, and room temperature is cooled to after reaction completely, are filtered off except mantoquita, filtrate decompression essence
Dimethylformamide is reclaimed after evaporating, obtains 2- methyl -3- chloroanisoles；
B. added in another reactor by appropriate butyl oxide and magnesium, temperature control added at 30 DEG C~60 DEG C bromoethanes and
The mixed liquor of 2- methyl -3- chloroanisoles, after reacting 20min~40min, 2- first is added dropwise at 40 DEG C~60 DEG C in temperature control
Base -3- chloroanisoles, rear insulation reaction 1.5h~2.5h is added dropwise, is subsequently cooled to -15 DEG C~-5 DEG C, it is dry by batch addition
Then ice, temperature control are poured into reaction solution in frozen water in 0 DEG C~20 DEG C insulation reaction 2h~4h, acid adding adjusts ph values to 1,
Reclaim butyl oxide after layering in organic layer, then in residue plus alkali adjusts ph values to 12, decolourized with activated carbon, filtrate
Acid adding adjusts ph values to 1, and it is 2- methyl -3- methoxy benzoic acids to separate out white powder.
In the step B, the parts by weight of butyl oxide are 700~900, and the parts by weight of magnesium are 30~50, the parts by weight of dry ice
For 70~80, the parts by weight of bromoethane are 2~4；2- first in the mixed liquor of bromoethane and 2- the methyl -3- chloroanisoles
The parts by weight of base -3- chloroanisoles are 1~2, and the parts by weight for the 2- methyl -3- chloroanisoles being added dropwise are 248~249.
The cuprous salt is stannous chloride or cuprous cyanide.
The concentration of the sodium methoxide solution is 30%.
The acid that ph values are adjusted in the step B is the hydrochloric acid solution that concentration is 10%.
The alkali that ph values are adjusted in the step B is the sodium hydroxide solution that concentration is 5%.
White powder is separated out in the step B and obtains finished product after centrifuge dripping is dried.
The mol ratio of the 2,6- dichlorotoleune and sodium methoxide is the ︰ 0.9 of 1 ︰ 1.35~1.
The quality of the cuprous salt is the 0.2%~0.5% of 2,6- dichlorotoleune and sodium methoxide gross mass.
The quality of the dimethylformamide is 60%~100% to 2,6- dichlorotoleune and sodium methoxide gross mass.
The present invention has positive effect：The synthetic method of the 2- methyl -3- methoxy benzoic acids of the present invention is with sodium methoxide
It is that raw material route is succinct with 2,6-DCT, reaction process is short, and dimethylformamide and butyl oxide are easily recycled as solvent,
It can be utilized with iterative cycles, and yield can be effectively improved, advantageously reduce cost.2- methyl -3- the methoxybenzenes of the present invention
The synthetic method of formic acid is suitable to industrial mass production.
Embodiment
Embodiment 1
The specific steps of the synthetic method of the 2- methyl -3- methoxy benzoic acids of the present embodiment include：
A. sodium methoxide solution 180kg, 2,6- dichlorotoleune 161kg, dimethylformamide that concentration is 30% are added in a kettle
161kg and stannous chloride 0.5kg, stirring heating, temperature control are reacted at 100 DEG C, and room temperature, mistake are cooled to after reacting 16h
Elimination removes mantoquita, reclaims dimethylformamide after filtrate decompression rectifying, obtains the 2- methyl -3- chloroanisole liquid of water white transparency
Body.Step A reaction equation（1）It is as follows：
B. in another reactor add butyl oxide 400kg and magnesium 20kg, temperature control 40 DEG C add 1kg bromoethanes and
The mixed liquor of 0.5kg 2- methyl -3- chloroanisoles, after reacting 30min, 2- methyl -3- chlorine is added dropwise at 50 DEG C for temperature control
Methyl phenyl ethers anisole 124.5kg, rear insulation reaction 2h is added dropwise, is subsequently cooled to -10 DEG C, dry ice 35kg, temperature control are added by batch
In 10 DEG C of insulation reaction 3h, then reaction solution is poured into frozen water, adds the hydrochloric acid solution that concentration is 10% to adjust ph values to 1, is layered
Butyl oxide is reclaimed in organic layer afterwards, then adds the sodium hydroxide solution that concentration is 5% to adjust ph values to 12 in residue, with work
Property charcoal decolourized, filtrate adds the hydrochloric acid solution that concentration is 10% to adjust ph values to 1, separates out white powder, centrifuge dripping, dries
After obtain finished product 2- methyl -3- methoxy benzoic acids, measure actual content as 98.8%.Step B reaction equation（2）It is as follows：
Embodiment 2
The specific steps of the synthetic method of the 2- methyl -3- methoxy benzoic acids of the present embodiment include：
A. sodium methoxide solution 270kg, 2,6- dichlorotoleune 161kg, dimethylformamide that concentration is 30% are added in a kettle
200kg and stannous chloride 0.5kg, stirring heating, temperature control are reacted at 120 DEG C, and room temperature, mistake are cooled to after reacting 15h
Elimination removes mantoquita, reclaims dimethylformamide after filtrate decompression rectifying, obtains the 2- methyl -3- chloroanisole liquid of water white transparency
Body.
B. butyl oxide 400kg and magnesium 20kg is added in another reactor, temperature control adds 1kg bromoethanes at 45 DEG C
With the mixed liquor of 0.5kg 2- methyl -3- chloroanisoles, after reacting 40min, 2- methyl -3- is added dropwise at 55 DEG C for temperature control
Chloroanisole 124.5kg, rear insulation reaction 2.5h is added dropwise, is subsequently cooled to -10 DEG C, dry ice 40kg, temperature are added by batch
Control in 20 DEG C of insulation reaction 2.5h, then pour into reaction solution in frozen water, add the hydrochloric acid solution that concentration is 10% to adjust ph values extremely
1, butyl oxide is reclaimed after layering in organic layer, then add the sodium hydroxide solution that concentration is 5% to adjust ph values extremely in residue
12, decolourized with activated carbon, filtrate adds the hydrochloric acid solution that concentration is 10% to adjust ph values to 1, separates out white powder, centrifugal drying
It is dry, finished product 2- methyl -3- methoxy benzoic acids are obtained after drying, measure actual content as 98.3%.
Embodiment 3
The specific steps of the synthetic method of the 2- methyl -3- methoxy benzoic acids of the present embodiment include：
A. sodium methoxide solution 240kg, 2,6- dichlorotoleune 161kg, dimethylformamide that concentration is 30% are added in a kettle
180kg and cuprous cyanide 0.5kg, stirring heating, temperature control are reacted at 110 DEG C, and room temperature, mistake are cooled to after reaction completely
Elimination removes mantoquita, reclaims dimethylformamide after filtrate decompression rectifying, obtains the 2- methyl -3- chloroanisole liquid of water white transparency
Body.
B. butyl oxide 400kg and magnesium 20kg is added in another reactor, temperature control adds 1kg bromoethanes at 40 DEG C
With the mixed liquor of 0.5kg 2- methyl -3- chloroanisoles, after reacting 40min, 2- methyl -3- is added dropwise at 45 DEG C for temperature control
Chloroanisole 124.5kg, rear insulation reaction 2.5h is added dropwise, is subsequently cooled to -10 DEG C, dry ice 35kg, temperature are added by batch
Then control is poured into reaction solution in frozen water in 10 DEG C of insulation reaction 3h, add the hydrochloric acid solution that concentration is 10% to adjust ph values to 1,
Reclaim butyl oxide after layering in organic layer, then in residue plus sodium hydroxide solution that concentration is 5% adjusts ph values to 12,
To be decolourized with activated carbon, filtrate adds the hydrochloric acid solution that concentration is 10% to adjust ph values to 1, separates out white powder, centrifuge dripping,
Finished product 2- methyl -3- methoxy benzoic acids are obtained after drying, measure actual content as 99.1%.
Raw materials used in the present invention is bought-in article unless otherwise specified, and concentration is that chemistry is pure.
Obviously, above-described embodiment is only intended to clearly illustrate example of the present invention, and is not to the present invention
The restriction of embodiment.For those of ordinary skill in the field, it can also be made on the basis of the above description
Its various forms of changes or variation.There is no necessity and possibility to exhaust all the enbodiments.And these belong to this hair
Among the obvious changes or variations that bright spirit is extended out is still in protection scope of the present invention.
Claims (10)
1. a kind of synthetic method of 2- methyl -3- methoxy benzoic acids, it is characterised in that specific steps include：
A. appropriate sodium methoxide solution, 2,6- dichlorotoleune, dimethylformamide and cuprous salt stirring is added in a kettle to rise
Temperature, temperature control are reacted at 80 DEG C~150 DEG C, and room temperature is cooled to after reaction completely, are filtered off except mantoquita, filtrate decompression essence
Dimethylformamide is reclaimed after evaporating, obtains 2- methyl -3- chloroanisoles；
B. added in another reactor by appropriate butyl oxide and magnesium, temperature control added at 30 DEG C~60 DEG C bromoethanes and
The mixed liquor of 2- methyl -3- chloroanisoles, after reacting 20min~40min, 2- first is added dropwise at 40 DEG C~60 DEG C in temperature control
Base -3- chloroanisoles, rear insulation reaction 1.5h~2.5h is added dropwise, is subsequently cooled to -15 DEG C~-5 DEG C, it is dry by batch addition
Then ice, temperature control are poured into reaction solution in frozen water in 0 DEG C~20 DEG C insulation reaction 2h~4h, acid adding adjusts ph values to 1,
Reclaim butyl oxide after layering in organic layer, then in residue plus alkali adjusts ph values to 12, decolourized with activated carbon, filtrate
Acid adding adjusts ph values to 1, and it is 2- methyl -3- methoxy benzoic acids to separate out white powder.
A kind of 2. synthetic method of 2- methyl -3- methoxy benzoic acids according to claim 1, it is characterised in that：It is described
In step B, the parts by weight of butyl oxide are 700~900, and the parts by weight of magnesium are 30~50, and the parts by weight of dry ice are 70~80, bromine second
The parts by weight of alkane are 2~4；2- methyl -3- chloroanisoles in the mixed liquor of bromoethane and 2- the methyl -3- chloroanisoles
Parts by weight are 1~2, and the parts by weight for the 2- methyl -3- chloroanisoles being added dropwise are 248~249.
A kind of 3. synthetic method of 2- methyl -3- methoxy benzoic acids according to claim 2, it is characterised in that：It is described
Cuprous salt is stannous chloride or cuprous cyanide.
A kind of 4. synthetic method of 2- methyl -3- methoxy benzoic acids according to claim 1, it is characterised in that：It is described
The concentration of sodium methoxide solution is 30%.
A kind of 5. synthetic method of 2- methyl -3- methoxy benzoic acids according to claim 1, it is characterised in that：It is described
The acid that ph values are adjusted in step B is the hydrochloric acid solution that concentration is 10%.
A kind of 6. synthetic method of 2- methyl -3- methoxy benzoic acids according to claim 1, it is characterised in that：It is described
The alkali that ph values are adjusted in step B is the sodium hydroxide solution that concentration is 5%.
A kind of 7. synthetic method of 2- methyl -3- methoxy benzoic acids according to claim 1, it is characterised in that：It is described
White powder is separated out in step B and obtains finished product after centrifuge dripping is dried.
8. a kind of synthetic method of 2- methyl -3- methoxy benzoic acids according to any one of claim 1 to 7, it is special
Sign is：The mol ratio of the 2,6- dichlorotoleune and sodium methoxide is the ︰ 0.9 of 1 ︰ 1.35~1.
9. a kind of synthetic method of 2- methyl -3- methoxy benzoic acids according to any one of claim 1 to 7, it is special
Sign is：The quality of the cuprous salt is the 0.2%~0.5% of 2,6- dichlorotoleune and sodium methoxide gross mass.
10. a kind of synthetic method of 2- methyl -3- methoxy benzoic acids according to any one of claim 1 to 7, it is special
Sign is：The quality of the dimethylformamide is 60%~100% to 2,6- dichlorotoleune and sodium methoxide gross mass.
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| CN111018693A (en) * | 2020-01-02 | 2020-04-17 | 西安正阳嘉禾化工科技有限公司 | 2-methyl-3-methoxybenzoic acid and preparation method thereof |
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| CN1188107A (en) * | 1996-09-24 | 1998-07-22 | 罗姆和哈斯公司 | Process for synthesizing benzoic acids |
| EP1044980A1 (en) * | 1997-12-09 | 2000-10-18 | Ihara Chemical Industry Co., Ltd. | Process for producing toluene derivatives |
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| Title |
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| 崔茹平: "3-甲氧基-2-甲基苯甲酸的合成研究", 《广东化工》 * |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN111018693A (en) * | 2020-01-02 | 2020-04-17 | 西安正阳嘉禾化工科技有限公司 | 2-methyl-3-methoxybenzoic acid and preparation method thereof |
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