YU6200A - Postupak za proizvodnju diestara 2,3,5-trimetilhidrohinona - Google Patents
Postupak za proizvodnju diestara 2,3,5-trimetilhidrohinonaInfo
- Publication number
- YU6200A YU6200A YU6200A YUP6200A YU6200A YU 6200 A YU6200 A YU 6200A YU 6200 A YU6200 A YU 6200A YU P6200 A YUP6200 A YU P6200A YU 6200 A YU6200 A YU 6200A
- Authority
- YU
- Yugoslavia
- Prior art keywords
- trimethylhydrochinon
- diesters
- producing
- acid
- trimethylhydrochinondiesters
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 2
- 150000005690 diesters Chemical class 0.000 title 1
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 abstract 2
- 239000002253 acid Substances 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- 241000551547 Dione <red algae> Species 0.000 abstract 1
- 229930003427 Vitamin E Natural products 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 230000000996 additive effect Effects 0.000 abstract 1
- 230000015572 biosynthetic process Effects 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 abstract 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 238000007127 saponification reaction Methods 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 230000009466 transformation Effects 0.000 abstract 1
- 229940046009 vitamin E Drugs 0.000 abstract 1
- 235000019165 vitamin E Nutrition 0.000 abstract 1
- 239000011709 vitamin E Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/582—Recycling of unreacted starting or intermediate materials
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Liquid Crystal Substances (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Pronalazak se odnosi na poboljšani postupak za proizvodnju diestara 2,3,5-trimetil-hidrohinona pretvaranjem 2,6,6-trimetilcikloheks-2-en-1,4-diona (4-okso-izoforona, ketoizoforona) u prisustvu jednog rastvorenog, kiselog katalizatora i jednog sredstva za aciliranje, kao na pr. anhidrida karbonske kiseline ili halogenida karbonske kiseline. Diestar 2,3,5-trimetilhidrohinona može se, u datom slučaju, posle toga prevesti saponifikacijom u slobodan 2,3,5-trimetilhidrohinon (TMHQ), koji je vredan sastojak u sintezi vitamina E.[This invention refers to the improved procedure for the production of 2, 3, 5 -trimethylhydrochinondiesters with transformation of 2.6.6-trimethylcycloheks-2-en 1.4 diones (4-oxo-isoforones, ketoisoforones) in the presence of one dissolved, acid katalyst and one means for acilation, for example unhydrides of carbonic acid or halogenides of carbon acid. Diesther of 2.3.5 trimethylhydrochinon, can, in this concrete case, be later translated by saponification in free 2.3.5 trimethylhydrochinon (TMHQ), that is valuable additive in the synthesis of vitamin E.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19905685A DE19905685A1 (de) | 1999-02-11 | 1999-02-11 | Verfahren zur Herstellung von 2,3,5-Trimethylhydrochinondiestern |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| YU6200A true YU6200A (sh) | 2002-03-18 |
Family
ID=7897163
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| YU6200A YU6200A (sh) | 1999-02-11 | 2000-02-04 | Postupak za proizvodnju diestara 2,3,5-trimetilhidrohinona |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6417409B1 (sh) |
| EP (1) | EP1028103B1 (sh) |
| JP (1) | JP2000229909A (sh) |
| CN (1) | CN1265390A (sh) |
| AT (1) | ATE223369T1 (sh) |
| BR (1) | BR0000356A (sh) |
| CA (1) | CA2298740A1 (sh) |
| DE (2) | DE19905685A1 (sh) |
| DK (1) | DK1028103T3 (sh) |
| ES (1) | ES2182740T3 (sh) |
| ID (1) | ID25771A (sh) |
| IL (1) | IL134454A0 (sh) |
| IN (1) | IN187710B (sh) |
| YU (1) | YU6200A (sh) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100374408C (zh) | 2001-12-14 | 2008-03-12 | Dsmip资产有限公司 | 三甲基氢醌二酰化物的制备 |
| DE602004014290D1 (de) * | 2003-11-07 | 2008-07-17 | Dsm Ip Assets Bv | Verfahren zur herstellung von 2,3,5-trimethylhydrochinondiacylaten |
| CN111675612B (zh) * | 2020-06-16 | 2023-03-03 | 万华化学集团股份有限公司 | 一种制备2,3,5-三甲基氢醌二酯的方法 |
| CN115850063B (zh) * | 2022-12-08 | 2025-05-13 | 万华化学集团股份有限公司 | 一种2,3,5-三甲基氢醌二酯的制备方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| UST900015I4 (en) * | 1970-10-01 | 1972-07-25 | defensive publication | |
| FR2327980A1 (fr) * | 1975-10-14 | 1977-05-13 | Rhone Poulenc Ind | Procede de preparation de trimethylhydroquinone |
| ES2162147T3 (es) * | 1996-05-14 | 2001-12-16 | Degussa | Procedimiento para la preparacion de trimetilhidroquinona. |
| EP0850912B1 (en) * | 1996-12-27 | 2001-11-07 | Daicel Chemical Industries, Ltd. | Method for producing trimethylcatechol diester |
| DE69708450T2 (de) * | 1996-12-27 | 2002-05-16 | Daicel Chemical Industries, Ltd. | Methode zum Herstellen von Trimethylhydroquinondiester |
-
1999
- 1999-02-11 DE DE19905685A patent/DE19905685A1/de not_active Withdrawn
-
2000
- 2000-01-28 ES ES00101759T patent/ES2182740T3/es not_active Expired - Lifetime
- 2000-01-28 AT AT00101759T patent/ATE223369T1/de not_active IP Right Cessation
- 2000-01-28 DE DE50000430T patent/DE50000430D1/de not_active Expired - Fee Related
- 2000-01-28 DK DK00101759T patent/DK1028103T3/da active
- 2000-01-28 EP EP00101759A patent/EP1028103B1/de not_active Expired - Lifetime
- 2000-02-01 IN IN51CA2000 patent/IN187710B/en unknown
- 2000-02-02 ID IDP20000075D patent/ID25771A/id unknown
- 2000-02-04 CN CN00101990A patent/CN1265390A/zh active Pending
- 2000-02-04 YU YU6200A patent/YU6200A/sh unknown
- 2000-02-09 JP JP2000032218A patent/JP2000229909A/ja active Pending
- 2000-02-09 IL IL13445400A patent/IL134454A0/xx unknown
- 2000-02-10 BR BR0000356-5A patent/BR0000356A/pt not_active IP Right Cessation
- 2000-02-10 CA CA002298740A patent/CA2298740A1/en not_active Abandoned
- 2000-02-11 US US09/502,229 patent/US6417409B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP1028103A1 (de) | 2000-08-16 |
| CN1265390A (zh) | 2000-09-06 |
| DE19905685A1 (de) | 2000-08-17 |
| ID25771A (id) | 2000-11-02 |
| IL134454A0 (en) | 2001-04-30 |
| BR0000356A (pt) | 2000-08-15 |
| JP2000229909A (ja) | 2000-08-22 |
| ES2182740T3 (es) | 2003-03-16 |
| EP1028103B1 (de) | 2002-09-04 |
| DE50000430D1 (de) | 2002-10-10 |
| IN187710B (sh) | 2002-06-08 |
| DK1028103T3 (da) | 2003-01-06 |
| CA2298740A1 (en) | 2000-08-11 |
| ATE223369T1 (de) | 2002-09-15 |
| US6417409B1 (en) | 2002-07-09 |
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