CA2327890A1 - Procede d'oxydation au moyen de tempo - Google Patents
Procede d'oxydation au moyen de tempo Download PDFInfo
- Publication number
- CA2327890A1 CA2327890A1 CA002327890A CA2327890A CA2327890A1 CA 2327890 A1 CA2327890 A1 CA 2327890A1 CA 002327890 A CA002327890 A CA 002327890A CA 2327890 A CA2327890 A CA 2327890A CA 2327890 A1 CA2327890 A1 CA 2327890A1
- Authority
- CA
- Canada
- Prior art keywords
- recited
- substituted
- unsubstituted
- cycloalkyl
- alkyl
- 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.)
- Abandoned
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
- C07C201/12—Preparation of nitro compounds by reactions not involving the formation of nitro groups
-
- 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
- C07C227/02—Formation of carboxyl groups in compounds containing amino groups, e.g. by oxidation of amino alcohols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/29—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with halogen-containing compounds which may be formed in situ
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/52—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings condensed with carbocyclic rings or ring systems
- C07D263/54—Benzoxazoles; Hydrogenated benzoxazoles
- C07D263/56—Benzoxazoles; Hydrogenated benzoxazoles with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 2
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
L'invention concerne l'oxydation d'un alcool primaire représenté par la formule II en l'acide carboxylique représenté par la formule (I): R?1¿CH¿2?OH?R?1¿CO¿2?H.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US8120298P | 1998-04-09 | 1998-04-09 | |
US60/081,202 | 1998-04-09 | ||
GB9810188.4 | 1998-05-13 | ||
GBGB9810188.4A GB9810188D0 (en) | 1998-05-13 | 1998-05-13 | Oxidation process using TEMPO |
PCT/US1999/007466 WO1999052849A1 (fr) | 1998-04-09 | 1999-04-05 | Procede d'oxydation au moyen de tempo |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2327890A1 true CA2327890A1 (fr) | 1999-10-21 |
Family
ID=26313666
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002327890A Abandoned CA2327890A1 (fr) | 1998-04-09 | 1999-04-05 | Procede d'oxydation au moyen de tempo |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1070039A1 (fr) |
JP (1) | JP2002511440A (fr) |
AU (1) | AU748207B2 (fr) |
CA (1) | CA2327890A1 (fr) |
WO (1) | WO1999052849A1 (fr) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2003516939A (ja) * | 1999-11-08 | 2003-05-20 | エスシーエイ・ハイジーン・プロダクツ・ゼイスト・ベー・ブイ | 第一級アルコールを酸化する方法 |
JP2002371044A (ja) * | 2001-04-11 | 2002-12-26 | Ajinomoto Co Inc | β−アミノ−α−ヒドロキシカルボン酸の製造方法 |
JPWO2003016278A1 (ja) * | 2001-08-21 | 2004-12-02 | 藤沢薬品工業株式会社 | ピペリジン−2−イル酢酸の製造法 |
US6426418B1 (en) * | 2001-11-02 | 2002-07-30 | Apotex, Inc. | Processes for the manufacturing of 3-hydroxy-N,1,6-trialkyl-4-oxo-1,4-dihydropyridine-2-carboxamide |
DE10206619B4 (de) * | 2002-02-15 | 2004-03-25 | Consortium für elektrochemische Industrie GmbH | Verfahren zur Herstellung von Alkincarbonsäuren und Alkincarbonsäure-Alkinalkoholestern durch Oxidation von Alkinalkoholen |
DE10244633B3 (de) | 2002-09-25 | 2004-02-26 | Consortium für elektrochemische Industrie GmbH | Verfahren zur Herstellung von Alkincarbonsäuren durch Oxidation von Alkinalkoholen |
DE102004019376A1 (de) | 2004-04-21 | 2005-11-10 | Wacker-Chemie Gmbh | Verfahren zur Herstellung von Carboxyreste aufweisenden Organosiliciumverbindungen |
JP5274764B2 (ja) * | 2006-11-08 | 2013-08-28 | 広栄化学工業株式会社 | N−置換−ホルミルポリメチレンイミンの製造方法 |
EP2216345B1 (fr) * | 2007-11-26 | 2014-07-02 | The University of Tokyo | Nanofibre de cellulose et son procede de fabrication, et dispersion de nanofibre de cellulose |
GB0918616D0 (en) * | 2009-10-23 | 2009-12-09 | 3M Innovative Properties Co | Method of preparing highly fluorinated carboxylic acids and their salts |
WO2013078172A1 (fr) * | 2011-11-23 | 2013-05-30 | The United States Of America As Represented By The Secretary Of The Navy | Glycoconjugaison médiée par tempo d'une composition immunogène contre campylobacter jejuni |
CN104557579B (zh) * | 2014-12-09 | 2017-02-22 | 杭州海尔希畜牧科技有限公司 | 一种制备甜菜碱的方法 |
CN118660972A (zh) | 2022-02-11 | 2024-09-17 | 汉高股份有限及两合公司 | 用于合成α-亚甲基-γ-丁内酯的方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5631366A (en) * | 1995-01-12 | 1997-05-20 | Hoffmann-La Roche Inc. | Process for making 3-formylcephem derivatives |
-
1999
- 1999-04-05 JP JP2000543412A patent/JP2002511440A/ja not_active Withdrawn
- 1999-04-05 AU AU34711/99A patent/AU748207B2/en not_active Ceased
- 1999-04-05 WO PCT/US1999/007466 patent/WO1999052849A1/fr not_active Application Discontinuation
- 1999-04-05 EP EP99916376A patent/EP1070039A1/fr not_active Withdrawn
- 1999-04-05 CA CA002327890A patent/CA2327890A1/fr not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
AU3471199A (en) | 1999-11-01 |
JP2002511440A (ja) | 2002-04-16 |
AU748207B2 (en) | 2002-05-30 |
EP1070039A1 (fr) | 2001-01-24 |
WO1999052849A1 (fr) | 1999-10-21 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request | ||
FZDE | Dead |