ES2052137T3 - Proceso para la produccion de 3,4-epoxibutirato e intermediario para el mismo. - Google Patents
Proceso para la produccion de 3,4-epoxibutirato e intermediario para el mismo.Info
- Publication number
- ES2052137T3 ES2052137T3 ES90122398T ES90122398T ES2052137T3 ES 2052137 T3 ES2052137 T3 ES 2052137T3 ES 90122398 T ES90122398 T ES 90122398T ES 90122398 T ES90122398 T ES 90122398T ES 2052137 T3 ES2052137 T3 ES 2052137T3
- Authority
- ES
- Spain
- Prior art keywords
- formula
- epoxybutyrate
- compound
- group
- prepared
- 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 - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/01—Sulfonic acids
- C07C309/28—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/57—Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing carboxyl groups bound to the carbon skeleton
- C07C309/58—Carboxylic acid groups or esters thereof
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/38—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D303/40—Compounds containing oxirane rings with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals by ester radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/64—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms
- C07C309/65—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to acyclic carbon atoms of a saturated carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C07C309/63—Esters of sulfonic acids
- C07C309/72—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
- C07C309/73—Esters of sulfonic acids having sulfur atoms of esterified sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton to carbon atoms of non-condensed six-membered aromatic rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Epoxy Compounds (AREA)
Abstract
UN 3, 4-EPOXIBUTIRATO DE LA FORMULA: DONDE R ELEVADO 1 EN UN GRUPO ALCALINO O ARALCALINO PREPARADO EFICIENTEMENTE MEDIANTE UN PROCESO QUE COMPRENDE LOS PASOS SIGUIENTES: (A) REACCION 3, 4-DIHIDROXIBUTIRONITRILO DE LA FORMULA: CON UN CLORURO SULFONILO DE LA FORMULA: R (AL CUADRADO) -SO SUB 2 -CL DONDE R (AL CUADRADO) ES UN GRUPO ALCALINO O UN GRUPO FENILO QUE PUEDE SUSTITUIRSE EN PRESENCIA DE UNA BASE PARA OBTENER UN COMPUESTO DE LA FORMULA: (B) REACCION DEL COMPUESTO PREPARADO EN EL PASO (A) CON UN ALCOHOL DE LA FORMULA: R ELEVADO 1 -OH EN PRESENCIA DE UN ACIDO PARA OBTENER UN COMPUESTO DE LA FORMULA: Y (C) REACCION DEL COMPUESTO PREPARADO EN EL PASO (B) CON UNA BASE PARA OBTENER EL 3, 4-EPOXIBUTIRATO.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1305895A JP2834501B2 (ja) | 1989-11-25 | 1989-11-25 | 3,4―エポキシ酪酸エステルの製法および中間体 |
Publications (1)
Publication Number | Publication Date |
---|---|
ES2052137T3 true ES2052137T3 (es) | 1994-07-01 |
Family
ID=17950597
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ES90122398T Expired - Lifetime ES2052137T3 (es) | 1989-11-25 | 1990-11-23 | Proceso para la produccion de 3,4-epoxibutirato e intermediario para el mismo. |
Country Status (6)
Country | Link |
---|---|
US (1) | US5079382A (es) |
EP (1) | EP0430096B1 (es) |
JP (1) | JP2834501B2 (es) |
KR (1) | KR0163770B1 (es) |
DE (1) | DE69007028T2 (es) |
ES (1) | ES2052137T3 (es) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0657446B1 (en) * | 1993-12-06 | 1998-05-13 | Nippon Kayaku Kabushiki Kaisha | Process for producing optically active erythro-3-amino-1,2-epoxy compound |
KR100247563B1 (ko) * | 1997-07-16 | 2000-04-01 | 박영구 | 키랄3,4-에폭시부티르산및이의염의제조방법 |
EP1052257B1 (en) | 1998-01-28 | 2004-03-31 | Nippon Kayaku Kabushiki Kaisha | Process for producing optically active threo-3-amino-1,2-epoxy compounds |
KR100332703B1 (ko) * | 1998-07-24 | 2002-08-27 | 삼성정밀화학 주식회사 | 광학활성을갖는(s)-3,4-에폭시부티르산염의제조방법 |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA1037964A (en) * | 1973-02-14 | 1978-09-05 | Eugene R. Wagner | 2-((3,5-di-tert-buryl-4-hydroxyphenyl)thio)alkanoic acids and derivatives and esters |
DK154886C (da) * | 1978-06-27 | 1989-05-16 | Merck & Co Inc | Fremgangsmaade til fremstilling af epihalogenhydrin-enantiomere |
FR2479192A1 (fr) * | 1980-03-28 | 1981-10-02 | Roussel Uclaf | Procede de preparation de derives cyclopropaniques tetra-substitues |
IT1184284B (it) * | 1985-06-28 | 1987-10-22 | Sigma Tau Ind Farmaceuti | Procedimento per la preparazione di r(-)-norcarnitina terz-butil estere |
JPH0723356B2 (ja) * | 1987-10-30 | 1995-03-15 | 帝人株式会社 | 4,4―ジスルホニルブタン酸エステル類の製造法 |
US4937235A (en) * | 1989-01-23 | 1990-06-26 | American Cyanamid Company | 3- or 4-substituted oxotremorine derivatives |
US4966731A (en) * | 1990-01-12 | 1990-10-30 | Monsanto Company | Process for preparing sulfonyl acids |
-
1989
- 1989-11-25 JP JP1305895A patent/JP2834501B2/ja not_active Expired - Fee Related
-
1990
- 1990-11-23 US US07/617,345 patent/US5079382A/en not_active Expired - Fee Related
- 1990-11-23 DE DE69007028T patent/DE69007028T2/de not_active Expired - Fee Related
- 1990-11-23 ES ES90122398T patent/ES2052137T3/es not_active Expired - Lifetime
- 1990-11-23 EP EP90122398A patent/EP0430096B1/en not_active Expired - Lifetime
- 1990-11-24 KR KR1019900019118A patent/KR0163770B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
DE69007028D1 (de) | 1994-04-07 |
EP0430096A2 (en) | 1991-06-05 |
JPH03167167A (ja) | 1991-07-19 |
EP0430096A3 (en) | 1991-12-27 |
JP2834501B2 (ja) | 1998-12-09 |
US5079382A (en) | 1992-01-07 |
KR910009647A (ko) | 1991-06-28 |
KR0163770B1 (ko) | 1999-01-15 |
EP0430096B1 (en) | 1994-03-02 |
DE69007028T2 (de) | 1994-08-04 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FG2A | Definitive protection |
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