KR100468237B1 - 멘톨의 제조방법 - Google Patents
멘톨의 제조방법 Download PDFInfo
- Publication number
- KR100468237B1 KR100468237B1 KR10-2000-0030101A KR20000030101A KR100468237B1 KR 100468237 B1 KR100468237 B1 KR 100468237B1 KR 20000030101 A KR20000030101 A KR 20000030101A KR 100468237 B1 KR100468237 B1 KR 100468237B1
- Authority
- KR
- South Korea
- Prior art keywords
- menthol
- boric acid
- mentone
- reacting
- peppermint
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- NOOLISFMXDJSKH-UHFFFAOYSA-N DL-menthol Natural products CC(C)C1CCC(C)CC1O NOOLISFMXDJSKH-UHFFFAOYSA-N 0.000 title claims abstract description 19
- 229940041616 menthol Drugs 0.000 title claims abstract description 18
- 238000000034 method Methods 0.000 title claims abstract description 15
- NOOLISFMXDJSKH-UTLUCORTSA-N (+)-Neomenthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@@H]1O NOOLISFMXDJSKH-UTLUCORTSA-N 0.000 title description 13
- NOOLISFMXDJSKH-KXUCPTDWSA-N (-)-Menthol Chemical compound CC(C)[C@@H]1CC[C@@H](C)C[C@H]1O NOOLISFMXDJSKH-KXUCPTDWSA-N 0.000 claims abstract description 33
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims abstract description 24
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims abstract description 18
- 239000004327 boric acid Substances 0.000 claims abstract description 15
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims abstract description 14
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims abstract description 9
- 239000002184 metal Substances 0.000 claims abstract description 8
- 235000011121 sodium hydroxide Nutrition 0.000 claims abstract description 6
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims abstract description 5
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 6
- 238000004519 manufacturing process Methods 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 3
- 239000001525 mentha piperita l. herb oil Substances 0.000 claims 1
- 239000003921 oil Substances 0.000 claims 1
- 235000019198 oils Nutrition 0.000 claims 1
- 235000019477 peppermint oil Nutrition 0.000 claims 1
- 235000016257 Mentha pulegium Nutrition 0.000 abstract description 19
- 235000004357 Mentha x piperita Nutrition 0.000 abstract description 19
- 235000001050 hortel pimenta Nutrition 0.000 abstract description 19
- 244000246386 Mentha pulegium Species 0.000 abstract description 15
- 239000010779 crude oil Substances 0.000 abstract description 10
- 238000004508 fractional distillation Methods 0.000 abstract description 7
- 230000000694 effects Effects 0.000 abstract description 2
- 238000009835 boiling Methods 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 241001479543 Mentha x piperita Species 0.000 description 5
- 239000003205 fragrance Substances 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 230000005484 gravity Effects 0.000 description 4
- 239000002537 cosmetic Substances 0.000 description 3
- 235000013305 food Nutrition 0.000 description 3
- 239000012535 impurity Substances 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000000047 product Substances 0.000 description 3
- 238000000926 separation method Methods 0.000 description 3
- NOOLISFMXDJSKH-AEJSXWLSSA-N (+)-menthol Chemical compound CC(C)[C@H]1CC[C@H](C)C[C@@H]1O NOOLISFMXDJSKH-AEJSXWLSSA-N 0.000 description 2
- FOBXOZMHEKILEY-UHFFFAOYSA-N (-)-Aristolene Chemical compound C1C2C(C)(C)C2C2(C)C(C)CCCC2=C1 FOBXOZMHEKILEY-UHFFFAOYSA-N 0.000 description 2
- 241000196324 Embryophyta Species 0.000 description 2
- 239000006227 byproduct Substances 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- GRWFGVWFFZKLTI-UHFFFAOYSA-N α-pinene Chemical compound CC1=CCC2C(C)(C)C1C2 GRWFGVWFFZKLTI-UHFFFAOYSA-N 0.000 description 2
- WTARULDDTDQWMU-RKDXNWHRSA-N (+)-β-pinene Chemical compound C1[C@H]2C(C)(C)[C@@H]1CCC2=C WTARULDDTDQWMU-RKDXNWHRSA-N 0.000 description 1
- WTARULDDTDQWMU-IUCAKERBSA-N (-)-Nopinene Natural products C1[C@@H]2C(C)(C)[C@H]1CCC2=C WTARULDDTDQWMU-IUCAKERBSA-N 0.000 description 1
- ITYNGVSTWVVPIC-DHGKCCLASA-N (-)-allo-Aromadendrene Chemical compound C([C@@H]1[C@H]2C1(C)C)CC(=C)[C@@H]1[C@H]2[C@H](C)CC1 ITYNGVSTWVVPIC-DHGKCCLASA-N 0.000 description 1
- NFLGAXVYCFJBMK-IUCAKERBSA-N (-)-isomenthone Chemical compound CC(C)[C@@H]1CC[C@H](C)CC1=O NFLGAXVYCFJBMK-IUCAKERBSA-N 0.000 description 1
- YSTPAHQEHQSRJD-SECBINFHSA-N (-)-piperitone Chemical compound CC(C)[C@H]1CCC(C)=CC1=O YSTPAHQEHQSRJD-SECBINFHSA-N 0.000 description 1
- GRWFGVWFFZKLTI-IUCAKERBSA-N 1S,5S-(-)-alpha-Pinene Natural products CC1=CC[C@@H]2C(C)(C)[C@H]1C2 GRWFGVWFFZKLTI-IUCAKERBSA-N 0.000 description 1
- NEEKVKZFYBQFGT-BTJKTKAUSA-N 9-amino-1,2,3,4-tetrahydroacridin-1-ol;(z)-but-2-enedioic acid Chemical compound OC(=O)\C=C/C(O)=O.C1=CC=C2C(N)=C(C(O)CCC3)C3=NC2=C1 NEEKVKZFYBQFGT-BTJKTKAUSA-N 0.000 description 1
- ITYNGVSTWVVPIC-XGFWRYKXSA-N Alloaromadendrene Natural products C([C@@H]1[C@H]2C1(C)C)CC(=C)[C@@H]1[C@@H]2[C@H](C)CC1 ITYNGVSTWVVPIC-XGFWRYKXSA-N 0.000 description 1
- 241001465677 Ancylostomatoidea Species 0.000 description 1
- 201000004624 Dermatitis Diseases 0.000 description 1
- WEEGYLXZBRQIMU-UHFFFAOYSA-N Eucalyptol Chemical compound C1CC2CCC1(C)OC2(C)C WEEGYLXZBRQIMU-UHFFFAOYSA-N 0.000 description 1
- 208000018522 Gastrointestinal disease Diseases 0.000 description 1
- 206010019233 Headaches Diseases 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 1
- WTARULDDTDQWMU-UHFFFAOYSA-N Pseudopinene Natural products C1C2C(C)(C)C1CCC2=C WTARULDDTDQWMU-UHFFFAOYSA-N 0.000 description 1
- 206010037660 Pyrexia Diseases 0.000 description 1
- KXKVLQRXCPHEJC-UHFFFAOYSA-N acetic acid trimethyl ester Natural products COC(C)=O KXKVLQRXCPHEJC-UHFFFAOYSA-N 0.000 description 1
- XCPQUQHBVVXMRQ-UHFFFAOYSA-N alpha-Fenchene Natural products C1CC2C(=C)CC1C2(C)C XCPQUQHBVVXMRQ-UHFFFAOYSA-N 0.000 description 1
- MVNCAPSFBDBCGF-UHFFFAOYSA-N alpha-pinene Natural products CC1=CCC23C1CC2C3(C)C MVNCAPSFBDBCGF-UHFFFAOYSA-N 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 230000003110 anti-inflammatory effect Effects 0.000 description 1
- 230000002421 anti-septic effect Effects 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229930006722 beta-pinene Natural products 0.000 description 1
- 125000005619 boric acid group Chemical group 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 238000005119 centrifugation Methods 0.000 description 1
- 229930007050 cineol Natural products 0.000 description 1
- 229960005233 cineole Drugs 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001079 digestive effect Effects 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- LCWMKIHBLJLORW-UHFFFAOYSA-N gamma-carene Natural products C1CC(=C)CC2C(C)(C)C21 LCWMKIHBLJLORW-UHFFFAOYSA-N 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 231100000869 headache Toxicity 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 208000004296 neuralgia Diseases 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 230000000144 pharmacologic effect Effects 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000037394 skin elasticity Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 208000004371 toothache Diseases 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/76—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment
- C07C29/80—Separation; Purification; Use of additives, e.g. for stabilisation by physical treatment by distillation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/94—Use of additives, e.g. for stabilisation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
- C07C35/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic
- C07C35/08—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a six-membered rings
- C07C35/12—Menthol
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
Abstract
Description
성분 | 함량 | 성분 | 함량 |
알파-피넨(α-pinene) | 0.35% | 네오멘톨(neomenthol) | 2.30% |
캄페어(camphere) | 0.48% | 메틸 아세테이트(menthyl acetate) | 2.35% |
베타-피넨(β-pinene) | 2.29% | 멘톨(mentol) | 55.69% |
시네올(cineol) | 0.49% | 페페리톤(piperiton) | 6.32% |
멘톤(methon) | 19.26% | 아이소멘톤(iosmenthon) | 8.60% |
보우넨(bournene) | 0.55% | 알로아로마덴드렌(alloaromadendrene) | 1.28% |
아리스톨렌(aristolene) | 0.56% |
Claims (2)
- (a) 박하원유를 분별증류하여 L-멘톤만을 분리하여 제조하는 공정; (b) 상기 (a)공정에서 분리한 L-멘톤을 금속소다와 메틸알콜 존재하에 반응시켜 L-멘톨을 제조하는 공정; (c) 상기 (b) 공정에서 제조된 L-멘톨을 붕산과 반응시켜 붕산멘톨을 제조한 후 알콜로 처리하여 유분을 용해시킴으로써 이물질이 제거된 붕산멘톨을 제조하는 공정; (d) 상기 (c) 공정에서 제조한 붕산멘톨에 가성소다를 첨가하여 붕산을 분해시킴으로써 순수한 L-멘톨을 제조하는 공정을 포함하는 것을 특징으로 하는 L-멘톨 제조방법.
- 삭제
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2000-0030101A KR100468237B1 (ko) | 2000-06-01 | 2000-06-01 | 멘톨의 제조방법 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR10-2000-0030101A KR100468237B1 (ko) | 2000-06-01 | 2000-06-01 | 멘톨의 제조방법 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR20010109002A KR20010109002A (ko) | 2001-12-08 |
KR100468237B1 true KR100468237B1 (ko) | 2005-01-25 |
Family
ID=45855398
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR10-2000-0030101A Expired - Fee Related KR100468237B1 (ko) | 2000-06-01 | 2000-06-01 | 멘톨의 제조방법 |
Country Status (1)
Country | Link |
---|---|
KR (1) | KR100468237B1 (ko) |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3960970A (en) * | 1971-07-23 | 1976-06-01 | Basf Aktiengesellschaft | Manufacture of d,l-methol |
US5300706A (en) * | 1992-03-17 | 1994-04-05 | Bayer Aktiengesellschaft | Process for the preparation of d,1-menthol |
JPH08187039A (ja) * | 1995-01-10 | 1996-07-23 | Sanei Gen F F I Inc | l−メントールの収得方法 |
US5750803A (en) * | 1995-05-17 | 1998-05-12 | Bayer Aktiengesellschaft | Process for the preparation of D,L-menthol |
US5756864A (en) * | 1995-05-17 | 1998-05-26 | Bayer Aktiengesellschaft | Process for preparing D,L-menthol from D-menthol |
-
2000
- 2000-06-01 KR KR10-2000-0030101A patent/KR100468237B1/ko not_active Expired - Fee Related
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3960970A (en) * | 1971-07-23 | 1976-06-01 | Basf Aktiengesellschaft | Manufacture of d,l-methol |
US5300706A (en) * | 1992-03-17 | 1994-04-05 | Bayer Aktiengesellschaft | Process for the preparation of d,1-menthol |
JPH08187039A (ja) * | 1995-01-10 | 1996-07-23 | Sanei Gen F F I Inc | l−メントールの収得方法 |
US5750803A (en) * | 1995-05-17 | 1998-05-12 | Bayer Aktiengesellschaft | Process for the preparation of D,L-menthol |
US5756864A (en) * | 1995-05-17 | 1998-05-26 | Bayer Aktiengesellschaft | Process for preparing D,L-menthol from D-menthol |
Also Published As
Publication number | Publication date |
---|---|
KR20010109002A (ko) | 2001-12-08 |
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