CN100338020C - Tech. of preparing 2,4-dinitro methyl-phenoxide by nitro methyl-phenoxide interrupter nitration - Google Patents
Tech. of preparing 2,4-dinitro methyl-phenoxide by nitro methyl-phenoxide interrupter nitration Download PDFInfo
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- CN100338020C CN100338020C CNB2006100854939A CN200610085493A CN100338020C CN 100338020 C CN100338020 C CN 100338020C CN B2006100854939 A CNB2006100854939 A CN B2006100854939A CN 200610085493 A CN200610085493 A CN 200610085493A CN 100338020 C CN100338020 C CN 100338020C
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- Prior art keywords
- nitroanisole
- nitration
- dinitroanisole
- intermittent
- preparing
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- 238000006396 nitration reaction Methods 0.000 title claims abstract description 50
- GAKLFAZBKQGUBO-UHFFFAOYSA-N 2-methyl-3-nitrophenol Chemical compound CC1=C(O)C=CC=C1[N+]([O-])=O GAKLFAZBKQGUBO-UHFFFAOYSA-N 0.000 title 1
- LDWQQNOSQNSCTL-UHFFFAOYSA-N 3-methyl-2,4-dinitrophenol Chemical compound CC1=C([N+]([O-])=O)C=CC(O)=C1[N+]([O-])=O LDWQQNOSQNSCTL-UHFFFAOYSA-N 0.000 title 1
- BNUHAJGCKIQFGE-UHFFFAOYSA-N Nitroanisol Chemical compound COC1=CC=C([N+]([O-])=O)C=C1 BNUHAJGCKIQFGE-UHFFFAOYSA-N 0.000 claims abstract description 34
- 239000007788 liquid Substances 0.000 claims abstract description 28
- 239000000203 mixture Substances 0.000 claims abstract description 28
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims abstract description 24
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 claims abstract description 19
- 229910017604 nitric acid Inorganic materials 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 18
- 238000000926 separation method Methods 0.000 claims abstract description 17
- 238000002425 crystallisation Methods 0.000 claims abstract description 15
- CFBYEGUGFPZCNF-UHFFFAOYSA-N 2-nitroanisole Chemical compound COC1=CC=CC=C1[N+]([O-])=O CFBYEGUGFPZCNF-UHFFFAOYSA-N 0.000 claims abstract description 14
- 239000002253 acid Substances 0.000 claims abstract description 13
- 239000002994 raw material Substances 0.000 claims abstract description 13
- 230000008025 crystallization Effects 0.000 claims abstract description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 10
- 238000001816 cooling Methods 0.000 claims abstract description 7
- 239000012535 impurity Substances 0.000 claims abstract description 6
- CVYZVNVPQRKDLW-UHFFFAOYSA-N 2,4-dinitroanisole Chemical compound COC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O CVYZVNVPQRKDLW-UHFFFAOYSA-N 0.000 claims abstract 10
- 238000004519 manufacturing process Methods 0.000 claims abstract 6
- 238000002156 mixing Methods 0.000 claims abstract 3
- 239000012043 crude product Substances 0.000 claims description 8
- 230000018044 dehydration Effects 0.000 claims description 5
- 238000006297 dehydration reaction Methods 0.000 claims description 5
- 239000012847 fine chemical Substances 0.000 abstract description 2
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 abstract 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 abstract 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 30
- WDCYWAQPCXBPJA-UHFFFAOYSA-N 1,3-dinitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC([N+]([O-])=O)=C1 WDCYWAQPCXBPJA-UHFFFAOYSA-N 0.000 description 14
- 238000005516 engineering process Methods 0.000 description 14
- 238000002360 preparation method Methods 0.000 description 9
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000003756 stirring Methods 0.000 description 5
- JYMVSZGJZRQOFY-UHFFFAOYSA-N (4-nitrobenzoyl) 4-nitrobenzoate Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(=O)OC(=O)C1=CC=C([N+]([O-])=O)C=C1 JYMVSZGJZRQOFY-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 238000004064 recycling Methods 0.000 description 4
- SOFDTMPXXZJJMJ-UHFFFAOYSA-N (2-nitrobenzoyl) 2-nitrobenzoate Chemical compound [O-][N+](=O)C1=CC=CC=C1C(=O)OC(=O)C1=CC=CC=C1[N+]([O-])=O SOFDTMPXXZJJMJ-UHFFFAOYSA-N 0.000 description 3
- 238000000967 suction filtration Methods 0.000 description 3
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- 238000013019 agitation Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000006198 methoxylation reaction Methods 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 239000012065 filter cake Substances 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
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- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
本发明涉及一种硝基苯甲醚间歇硝化制备2，4-二硝基苯甲醚工艺，属于精细化工领域。本发明所述的工艺步骤如下：(1)硝化反应，分别以4-硝基苯甲醚、2-硝基苯甲醚、4-硝基苯甲醚和2-硝基苯甲醚混合物为原料与硝酸和硫酸混合而成的混酸发生间歇硝化反应；(2)液液分离，硝化反应结束后，进行液液分离，水相为中等浓度的混酸，油相中主要为2，4-二硝基苯甲醚，还有少量杂质及未反应的原料；(3)冷却结晶，在20℃～80℃温度下对油相进行冷却结晶，经固液分离，制备出2，4-二硝基苯甲醚粗品。本发明的好处是：(1)成本低；(2)工艺简单、工艺流程短；(3)安全、可靠性高；(4)可回收酸再利用。
The invention relates to a process for preparing 2,4-dinitroanisole by intermittent nitration of nitroanisole, which belongs to the field of fine chemicals. The process steps of the present invention are as follows: (1) nitration reaction, with 4-nitroanisole, 2-nitroanisole, 4-nitroanisole and 2-nitroanisole mixture as The mixed acid formed by mixing raw materials with nitric acid and sulfuric acid undergoes intermittent nitration reaction; (2) liquid-liquid separation, after the nitration reaction is completed, liquid-liquid separation is carried out, the water phase is a medium-concentration mixed acid, and the oil phase is mainly 2,4-Di Nitroanisole, and a small amount of impurities and unreacted raw materials; (3) Cooling crystallization, cooling and crystallizing the oil phase at a temperature of 20°C to 80°C, and preparing 2,4-dinitrate through solid-liquid separation crude anisole. The advantages of the invention are: (1) low cost; (2) simple process and short process flow; (3) high safety and reliability; (4) acid can be recovered and reused.
Description
Technical field
The present invention relates to the intermittently nitrated preparation 2 of a kind of Nitroanisole, 4-dinitrobenzene methyl ether technology belongs to field of fine chemical.
Background technology
2,4-dinitrobenzene methyl ether is important organic synthesis intermediate.Present 2, the preparation technology of 4-dinitrobenzene methyl ether is with 2, and the 4-dinitrochlorobenzene gets through methoxylation.This preparation technology drops into fused 2 in reactor, 4-dinitrochlorobenzene and sodium methylate are heated to about 40 ℃, and temperature is controlled at 58 ℃～60 ℃ and carries out methoxylation.After reaction finished, operation promptly got 2,4-dinitrobenzene methyl ether through separating treatment.But the main drawback that this processing method exists is: raw material 2, and the source of 4-dinitrochlorobenzene is well sold and in short supply, and this has caused the rising of product cost, and this technical process simultaneously is long, causes three-waste pollution easily.
Summary of the invention
The objective of the invention is at the deficiencies in the prior art, providing a kind of is the intermittently nitrated preparation 2 of Nitroanisole that raw material, technological process are simple, technical process is short with lower-cost Nitroanisole and composition thereof, 4-dinitrobenzene methyl ether technology.
The technical scheme that realizes above-mentioned purpose is: the intermittently nitrated preparation 2 of a kind of Nitroanisole, and 4-dinitrobenzene methyl ether technology, described processing step is as follows:
(1). nitration reaction is that intermittently nitration reaction takes place the nitration mixture that raw material and nitric acid and sulfuric acid mix with 4-Nitroanisole, 2-Nitroanisole, 4-Nitroanisole and 2-nitrobenzoyl ether mixture respectively;
(2). liquid liquid separates, and after nitration reaction finishes, carries out liquid liquid and separates, and water is the nitration mixture of intermediate concentration, is mainly 2 in the oil phase, and 4-dinitrobenzene methyl ether also has small amount of impurities and unreacted raw material;
(3). crystallisation by cooling, under 20 ℃～80 ℃ temperature, oil phase is carried out crystallisation by cooling, through solid-liquid separation, prepare 2,4-dinitrobenzene methyl ether crude product.
Further, the dehydration value of nitration mixture is controlled at 2.0～4.8 in the described the first step nitration reaction, and the mole proportioning of Nitroanisole and nitric acid is controlled at 1: 1.05～2.00, and the service temperature of nitration reaction is at 50 ℃～120 ℃.
Further, the isolating temperature of the described second step liquid liquid is controlled at 50 ℃～120 ℃.
Further, the solid-liquid separation temperature behind described the 3rd step crystallisation by cooling is controlled at 20 ℃～80 ℃.
Further, described nitration mixture is formed by 98% sulfuric acid, 95% nitric acid and the 65% nitric acid mixed preparing of technical grade.
Further, described nitration reaction is carried out in nitrator, and nitrator is the stirred-tank reactor that has heat-exchanger rig.
Further, described nitration reaction is carried out in nitrator, agitator in the nitrator is pusher impeller agitator, perhaps is hinged joint turbine type agitator, straight leaf disc formula turbine agitator, gear piece formula impeller agitator, flat leaf paddle agitator, crooked impeller-type stirrer.
Main chemical reactions formula of the present invention is:
Realize that the main technique equipment that the present invention needs is: stir nitrator, Crystallization Separation device and solid-liquid separator etc.
Reaction mechanism of the present invention is to adopt 2-Nitroanisole, 4-Nitroanisole and composition thereof to be raw material, generates 2,4-dinitrobenzene methyl ether.Because by the Location Mechanism of nitration reaction as can be known, on 2-Nitroanisole and 4-Nitroanisole phenyl ring-OCH
3Belong to the ortho para orientating group ,-NO
3Belong to meta-orienting group, these two orientating group orientation effect unanimities.Therefore, be reactant with 4-Nitroanisole, 2-Nitroanisole and 4-Nitroanisole and 2-nitrobenzoyl ether mixture, after the generation nitration reaction ,-NO
2Enter the position that they are determined jointly, promptly generate 2,4-dinitrobenzene methyl ether.In the nitrated generating process of 2-Nitroanisole, although 6 on the phenyl ring also are-OCH
3With-NO
3Co, but because 1-OCH
3With 2-NO
2Steric effect, so only may generate 2 of minute quantity, 6-dinitrobenzene methyl ether.In addition, 2, go up for 6 of 4-dinitrobenzene methyl ether phenyl ring nitration reaction further takes place, it is very difficult generating the 2 nitro.
Adopt the benefit of technique scheme to be: (1), cost are low.The present invention is to be that intermittently nitration reaction takes place the nitration mixture that raw material and nitric acid and sulfuric acid mix with 4-Nitroanisole, 2-Nitroanisole and 4-Nitroanisole and 2-nitrobenzoyl ether mixture, because Nitroanisole and mixture cost are lower, therefore prepare 2,4-dinitrobenzene methyl ether technology cost is low; (2), technology is simple, technical process is short.Technology of the present invention prepares 2 through nitration reaction, the separation of liquid liquid, crystallization separation process, 4-dinitrobenzene methyl ether crude product, and its technological process is simple, and technical process is short; (3), safety, reliability height.Because the whole technology of the present invention carries out at a lower temperature, cause the possibility of secondary pollution to descend greatly, so safety of the present invention, reliability height; (4) recyclable acid utilizes again.The present invention carries out liquid liquid and separates after nitration reaction takes place, and can carry out the recycling of acid to isolated water, this had both saved cost, has avoided the pollution of spent acid etc. again, very environmental protection.
Description of drawings
Accompanying drawing is a process flow sheet of the present invention.
Embodiment
The present invention is further detailed explanation below in conjunction with drawings and Examples.
Major equipment: stirred-tank reactor, Crystallization Separation device and the solid-liquid separator etc. that have heat-exchanger rig and pusher impeller agitator.
Embodiment one
The intermittently nitrated preparation 2 of a kind of Nitroanisole, 4-dinitrobenzene methyl ether technology, described processing step is as follows: in stirred-tank reactor, the 4-Nitroanisole is preheating to about 60 ℃, under agitation condition, nitration mixture under the room temperature is added drop-wise in the reactive system, nitration mixture is by 98% sulfuric acid of technical grade, 95% nitric acid and 65% nitric acid mixed preparing form, the dehydration value of nitration mixture is 4.2, the mole proportioning of Nitroanisole and nitric acid was controlled at 1.00: 1.05, control reaction temperature is at 65 ℃ ± 5 ℃, after dropwising, and heat temperature raising to 115 ℃ ± 5 ℃, constant temperature stirs 1.0h, leave standstill the layering of 1.0h liquid liquid then and separate, lower floor's water is a sulfuric acid, water and a spot of salpeter solution carry out can be recycled after the spent acid recycling; Upper oil phase is 2, and 4-dinitrobenzene methyl ether and a spot of 2 impurity and unreacted raw material 4-nitrobenzoyl ether mixture carry out Crystallization Separation.Be cooled to 60 ℃ of crystallizations, process suction filtration, prepare 2,4-dinitrobenzene methyl ether crude product.Obtain 2, conventional processing such as 4-dinitrobenzene methyl ether crude product can be washed, oven dry, can obtain lurid 2,4-dinitrobenzene methyl ether product.
Embodiment two
The intermittently nitrated preparation 2 of a kind of Nitroanisole, 4-dinitrobenzene methyl ether technology, described processing step is as follows: in stirred-tank reactor, the 2-Nitroanisole is heated to about 50 ℃, under agitation condition, nitration mixture under the room temperature is added drop-wise in the reactive system, nitration mixture is by 98% sulfuric acid of technical grade, 95% nitric acid and 65% nitric acid mixed preparing form, the dehydration value of nitration mixture is 4.7, the mole proportioning of Nitroanisole and nitric acid was controlled at 1.00: 1.10, control reaction temperature is at 70 ℃ ± 5 ℃, after dropwising, and heat temperature raising to 120 ℃ ± 5 ℃, constant temperature stirs 3.0h, leave standstill the layering of 1.0h liquid liquid then and separate, lower floor's water is a sulfuric acid, water and a spot of salpeter solution carry out can be recycled after the spent acid recycling; Upper oil phase is 2,4-dinitrobenzene methyl ether and a spot of 2, and 6-dinitrobenzene methyl ether and 2 impurity and unreacted raw material 2-Nitroanisole and 4-nitrobenzoyl ether mixture carry out Crystallization Separation.Be cooled to 30 ℃ of crystallizations, process suction filtration, prepare 2,4-dinitrobenzene methyl ether crude product.Obtain 2, conventional processing such as 4-dinitrobenzene methyl ether crude product can be washed, oven dry, can obtain lurid 2,4-dinitrobenzene methyl ether product.
Embodiment three
The intermittently nitrated preparation 2 of a kind of Nitroanisole, 4-dinitrobenzene methyl ether technology, described processing step is as follows: in stirred-tank reactor, 2-Nitroanisole and 4-nitrobenzoyl ether mixture are heated to about 60 ℃ as raw material, begin to add nitration mixture, nitration mixture is by 98% sulfuric acid of technical grade, 95% nitric acid and 65% nitric acid mixed preparing form, the dehydration value of nitration mixture is 2.8, and the mole proportioning of Nitroanisole and nitric acid was controlled at 1.00: 1.05, and temperature should maintain 55 ℃～75 ℃, after adding, continue to stir, when treating that temperature no longer rises, heat temperature raising degree to 120 ℃, and continue under 120 ℃ to stir 3.0h, two nitrated reactions can be finished.The layering of liquid liquid separates after leaving standstill 0.5h, and lower floor's water is sulfuric acid, water and a spot of salpeter solution, carries out can be recycled after the spent acid recycling; Upper oil phase is 2,4-dinitrobenzene methyl ether and a spot of 2, and 6-dinitrobenzene methyl ether and 2 impurity and unreacted raw material 2-Nitroanisole and 4-nitrobenzoyl ether mixture carry out Crystallization Separation.Be cooled to 60 ℃ of crystallizations, suction filtration while hot, prepare 2,4-dinitrobenzene methyl ether crude product.Filter cake conventional processing such as dries then with 70 ℃ of washings twice, can obtain lurid 2,4-dinitrobenzene methyl ether product.
Claims (7)
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|---|---|---|---|
| CNB2006100854939A CN100338020C (en) | 2006-06-19 | 2006-06-19 | Tech. of preparing 2,4-dinitro methyl-phenoxide by nitro methyl-phenoxide interrupter nitration |
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|---|---|---|---|
| CNB2006100854939A CN100338020C (en) | 2006-06-19 | 2006-06-19 | Tech. of preparing 2,4-dinitro methyl-phenoxide by nitro methyl-phenoxide interrupter nitration |
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| CN100338020C true CN100338020C (en) | 2007-09-19 |
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Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001077062A1 (en) * | 2000-04-11 | 2001-10-18 | Bayer Aktiengesellschaft | Method for producing 4-bromo- and 4-chloro-2-nitro-1-trifluoromethoxybenzene |
| CN1203045C (en) * | 2003-06-18 | 2005-05-25 | 江苏扬子江药业集团有限公司 | Method for preparing 4-chlorine-3-nitroanisole |
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- 2006-06-19 CN CNB2006100854939A patent/CN100338020C/en not_active Expired - Fee Related
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001077062A1 (en) * | 2000-04-11 | 2001-10-18 | Bayer Aktiengesellschaft | Method for producing 4-bromo- and 4-chloro-2-nitro-1-trifluoromethoxybenzene |
| CN1203045C (en) * | 2003-06-18 | 2005-05-25 | 江苏扬子江药业集团有限公司 | Method for preparing 4-chlorine-3-nitroanisole |
Non-Patent Citations (1)
| Title |
|---|
| 芳环上亲核取代反应──2．4-二硝基氯苯醚化的研究 曹瑞军，梅冬，西安交通大学学报，第8期 1994 * |
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