CN102844293B - 酮酯的氢化方法 - Google Patents
酮酯的氢化方法 Download PDFInfo
- Publication number
- CN102844293B CN102844293B CN201180019495.7A CN201180019495A CN102844293B CN 102844293 B CN102844293 B CN 102844293B CN 201180019495 A CN201180019495 A CN 201180019495A CN 102844293 B CN102844293 B CN 102844293B
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- CN
- China
- Prior art keywords
- solvent
- residue
- methods according
- formula
- binap
- 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.)
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/30—Preparation of optical isomers
- C07C227/32—Preparation of optical isomers by stereospecific synthesis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/02—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/04—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C229/22—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated the carbon skeleton being further substituted by oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
- C07C67/31—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by introduction of functional groups containing oxygen only in singly bound form
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
- C07C69/67—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids
- C07C69/675—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of saturated acids of saturated hydroxy-carboxylic acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33346210P | 2010-05-11 | 2010-05-11 | |
| EP10004966A EP2386536A1 (en) | 2010-05-11 | 2010-05-11 | A process for the hydrogenation of ketoesters |
| US61/333,462 | 2010-05-11 | ||
| EP10004966.7 | 2010-05-11 | ||
| PCT/EP2011/002323 WO2011141160A1 (en) | 2010-05-11 | 2011-05-10 | A process for the hydrogenation of ketoesters |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN102844293A CN102844293A (zh) | 2012-12-26 |
| CN102844293B true CN102844293B (zh) | 2016-01-27 |
Family
ID=42246339
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN201180019495.7A Active CN102844293B (zh) | 2010-05-11 | 2011-05-10 | 酮酯的氢化方法 |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US8431741B2 (enExample) |
| EP (2) | EP2386536A1 (enExample) |
| JP (1) | JP6018046B2 (enExample) |
| KR (1) | KR101848763B1 (enExample) |
| CN (1) | CN102844293B (enExample) |
| ES (1) | ES2567408T3 (enExample) |
| TW (1) | TWI519505B (enExample) |
| WO (1) | WO2011141160A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102633664B (zh) * | 2012-03-30 | 2014-05-28 | 广西新晶科技有限公司 | 一种左旋肉碱的制备方法 |
| CN102633705A (zh) * | 2012-03-31 | 2012-08-15 | 石家庄利康医药科技有限公司 | 一种制备奥拉西坦的方法 |
| CN103709058B (zh) * | 2013-12-10 | 2015-09-02 | 苏州汉酶生物技术有限公司 | 一种左旋肉碱的合成方法 |
| CN105218371A (zh) * | 2015-09-24 | 2016-01-06 | 上海交通大学 | 光学纯的3-羟基-4-(2,4,5-三氟苯基)丁酸乙酯的制备方法 |
| CN109851506B (zh) * | 2019-01-30 | 2020-09-15 | 凯特立斯(深圳)科技有限公司 | 钌-双膦催化剂催化的简单酮的不对称还原胺化制备手性伯胺 |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003097569A1 (en) * | 2002-05-22 | 2003-11-27 | Phoenix Chemicals Limited | Continuous process for the enantioselective catalytic hydrogenation of beta-ketoesters |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0699367B2 (ja) | 1987-06-11 | 1994-12-07 | 高砂香料工業株式会社 | 光学活性アルコ−ルの製法 |
| JPH0678277B2 (ja) | 1988-02-19 | 1994-10-05 | 高砂香料工業株式会社 | 光学活性アルコールおよびその誘導体の製造方法 |
| JPH0757758B2 (ja) | 1988-10-24 | 1995-06-21 | 高砂香料工業株式会社 | ルテニウム―ホスフィン錯体 |
| GB8911732D0 (en) | 1989-05-22 | 1989-07-05 | Ethyl Petroleum Additives Ltd | Lubricant compositions |
| IT1303757B1 (it) | 1998-11-16 | 2001-02-23 | Sigma Tau Ind Farmaceuti | Processo industriale per la produzione di l-carnitina. |
| NL1014280C2 (nl) * | 2000-02-03 | 2001-08-06 | Dsm Nv | Werkwijze voor de bereiding van melamine uit ureum. |
| JP4601779B2 (ja) * | 2000-07-25 | 2010-12-22 | 高砂香料工業株式会社 | 光学活性アルコールの製造方法 |
| GB2401864B (en) * | 2003-05-21 | 2007-11-14 | Phoenix Chemicals Ltd | Process and catalytic composition |
| EP1528053A1 (en) | 2003-10-31 | 2005-05-04 | Lonza Ag | Process for the preparation of (S)- or (R)-4-halo-3-hydroxybutyrates |
| US6939981B1 (en) * | 2004-06-25 | 2005-09-06 | Eastman Chemical Company | Ruthenium complexes of phosphine-aminophosphine ligands |
| JP2006206570A (ja) * | 2004-12-27 | 2006-08-10 | Nippon Synthetic Chem Ind Co Ltd:The | 光学活性β−ヒドロキシアミノ酸誘導体の製造方法 |
| CN101117304B (zh) * | 2006-08-03 | 2011-12-21 | 中国科学院化学研究所 | 一种进行不对称催化氢化反应的方法 |
| GB0822064D0 (en) * | 2008-12-03 | 2009-01-07 | Johnson Matthey Plc | Process for preparing cationic ruthenium complexes |
-
2010
- 2010-05-11 EP EP10004966A patent/EP2386536A1/en not_active Ceased
-
2011
- 2011-05-10 TW TW100116238A patent/TWI519505B/zh not_active IP Right Cessation
- 2011-05-10 US US13/104,114 patent/US8431741B2/en active Active
- 2011-05-10 EP EP11730183.8A patent/EP2569275B1/en active Active
- 2011-05-10 CN CN201180019495.7A patent/CN102844293B/zh active Active
- 2011-05-10 KR KR1020127029535A patent/KR101848763B1/ko active Active
- 2011-05-10 JP JP2013509468A patent/JP6018046B2/ja active Active
- 2011-05-10 WO PCT/EP2011/002323 patent/WO2011141160A1/en not_active Ceased
- 2011-05-10 ES ES11730183.8T patent/ES2567408T3/es active Active
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003097569A1 (en) * | 2002-05-22 | 2003-11-27 | Phoenix Chemicals Limited | Continuous process for the enantioselective catalytic hydrogenation of beta-ketoesters |
Non-Patent Citations (2)
| Title |
|---|
| A class of readily available optically pure 7,7"-disubstituted BINAPs for asymmetric catalysis;Wei-Cheng Yuan et al;《Tetrahedron》;20090523;第65卷(第21期);第4135页表8 * |
| Enantioselective hydrogenation of β-keto esters catalyzed bu chiral binaphthylbisphosphine ruthenium complexes;V.A.Pavlov et al;《Russian Chemical Bulletin》;20000430;第49卷(第4期);第728-731页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| KR101848763B1 (ko) | 2018-05-28 |
| ES2567408T3 (es) | 2016-04-22 |
| TWI519505B (zh) | 2016-02-01 |
| KR20130079394A (ko) | 2013-07-10 |
| EP2569275A1 (en) | 2013-03-20 |
| JP6018046B2 (ja) | 2016-11-02 |
| CN102844293A (zh) | 2012-12-26 |
| WO2011141160A1 (en) | 2011-11-17 |
| US8431741B2 (en) | 2013-04-30 |
| JP2013526493A (ja) | 2013-06-24 |
| EP2386536A1 (en) | 2011-11-16 |
| US20120016153A1 (en) | 2012-01-19 |
| TW201213280A (en) | 2012-04-01 |
| HK1179943A1 (zh) | 2013-10-11 |
| EP2569275B1 (en) | 2016-01-27 |
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