JPS57181039A - Preparation of oxocarboxylic acid ester - Google Patents
Preparation of oxocarboxylic acid esterInfo
- Publication number
- JPS57181039A JPS57181039A JP56064194A JP6419481A JPS57181039A JP S57181039 A JPS57181039 A JP S57181039A JP 56064194 A JP56064194 A JP 56064194A JP 6419481 A JP6419481 A JP 6419481A JP S57181039 A JPS57181039 A JP S57181039A
- Authority
- JP
- Japan
- Prior art keywords
- salt
- ruthenium
- preparation
- acid ester
- 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.)
- Granted
Links
- 239000002253 acid Substances 0.000 title 1
- 150000002148 esters Chemical class 0.000 title 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract 4
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical class [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- 150000003997 cyclic ketones Chemical class 0.000 abstract 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 abstract 2
- BGTOWKSIORTVQH-UHFFFAOYSA-N cyclopentanone Chemical compound O=C1CCCC1 BGTOWKSIORTVQH-UHFFFAOYSA-N 0.000 abstract 2
- VCJMYUPGQJHHFU-UHFFFAOYSA-N iron(3+);trinitrate Chemical compound [Fe+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VCJMYUPGQJHHFU-UHFFFAOYSA-N 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 239000002994 raw material Substances 0.000 abstract 2
- YAYGSLOSTXKUBW-UHFFFAOYSA-N ruthenium(2+) Chemical class [Ru+2] YAYGSLOSTXKUBW-UHFFFAOYSA-N 0.000 abstract 2
- 229910021578 Iron(III) chloride Inorganic materials 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- RBTARNINKXHZNM-UHFFFAOYSA-K iron trichloride Chemical compound Cl[Fe](Cl)Cl RBTARNINKXHZNM-UHFFFAOYSA-K 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 239000002304 perfume Substances 0.000 abstract 1
- -1 polymethylene Polymers 0.000 abstract 1
- WYRXRHOISWEUST-UHFFFAOYSA-K ruthenium(3+);tribromide Chemical compound [Br-].[Br-].[Br-].[Ru+3] WYRXRHOISWEUST-UHFFFAOYSA-K 0.000 abstract 1
- YBCAZPLXEGKKFM-UHFFFAOYSA-K ruthenium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Ru+3] YBCAZPLXEGKKFM-UHFFFAOYSA-K 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- FEONEKOZSGPOFN-UHFFFAOYSA-K tribromoiron Chemical compound Br[Fe](Br)Br FEONEKOZSGPOFN-UHFFFAOYSA-K 0.000 abstract 1
Classifications
-
- 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
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56064194A JPS57181039A (en) | 1981-04-30 | 1981-04-30 | Preparation of oxocarboxylic acid ester |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP56064194A JPS57181039A (en) | 1981-04-30 | 1981-04-30 | Preparation of oxocarboxylic acid ester |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS57181039A true JPS57181039A (en) | 1982-11-08 |
JPH0118889B2 JPH0118889B2 (enrdf_load_stackoverflow) | 1989-04-07 |
Family
ID=13251009
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP56064194A Granted JPS57181039A (en) | 1981-04-30 | 1981-04-30 | Preparation of oxocarboxylic acid ester |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS57181039A (enrdf_load_stackoverflow) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4649217A (en) * | 1982-04-02 | 1987-03-10 | Mitsubishi Chemical Industries Limited | Process for producing oxocarboxylic acids |
WO2007114199A1 (ja) * | 2006-03-28 | 2007-10-11 | Sumitomo Chemical Company, Limited | 光学活性(s)-7-ヒドロキシ-6-メチルヘプタン-2-オンおよびその前駆体の製造方法 |
JP2008099661A (ja) * | 2006-03-28 | 2008-05-01 | Sumitomo Chemical Co Ltd | 光学活性(s)−7−ヒドロキシ−6−メチルヘプタン−2−オンおよびその前駆体の製造方法 |
-
1981
- 1981-04-30 JP JP56064194A patent/JPS57181039A/ja active Granted
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4649217A (en) * | 1982-04-02 | 1987-03-10 | Mitsubishi Chemical Industries Limited | Process for producing oxocarboxylic acids |
WO2007114199A1 (ja) * | 2006-03-28 | 2007-10-11 | Sumitomo Chemical Company, Limited | 光学活性(s)-7-ヒドロキシ-6-メチルヘプタン-2-オンおよびその前駆体の製造方法 |
JP2008099661A (ja) * | 2006-03-28 | 2008-05-01 | Sumitomo Chemical Co Ltd | 光学活性(s)−7−ヒドロキシ−6−メチルヘプタン−2−オンおよびその前駆体の製造方法 |
US8026081B2 (en) | 2006-03-28 | 2011-09-27 | Sumitomo Chemical Company, Limited | Method of producing optically active (S)-7-hydroxy-6-methylheptan-2-one and precursor thereof |
Also Published As
Publication number | Publication date |
---|---|
JPH0118889B2 (enrdf_load_stackoverflow) | 1989-04-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JPS57181039A (en) | Preparation of oxocarboxylic acid ester | |
JPS5687527A (en) | Preparation of phenol | |
JPS5699254A (en) | Stabilized halogen-containing resin composition | |
JPS5630943A (en) | Preparation of lactic acid and/or its ester | |
JPS54125631A (en) | Preparation of high-purity terephthalic acid | |
JPS5657737A (en) | Preparation of cyclopropanecarboxylic acid ester | |
JPS5655444A (en) | Halogen-containing resin composition | |
JPS5538838A (en) | Preparation of polyester | |
JPS554325A (en) | Preparation of phenyl acetate and ketone | |
JPS574943A (en) | Preparation of carboxylic acid alkyl ester | |
JPS53130796A (en) | Preparation of polyester | |
JPS5548228A (en) | Preparation of stabilizer with reduced disagreeable odor | |
JPS5559128A (en) | Preparation of alkoxybenzaldehyde | |
JPS57183742A (en) | Production of 4-chloro-3-methylcrotyl ester | |
JPS5629542A (en) | Preparation of phenylacetic acid derivative | |
JPS57192326A (en) | Preparation of unsaturated carbonyl compound | |
JPS5683486A (en) | Preparation of 1,3-benzodioxol-5-ol | |
JPS54160338A (en) | Preparation of 2-methyl-2-(2-fluoro-4-biphenylyl)-malonic acid | |
JPS5540626A (en) | Preparation of 2-alkoxy-p-benzoquinone and 2-alkoxy-alpha-naphthoquinone | |
JPS57112400A (en) | Sterol saccharide and drug containing the same | |
JPS5639046A (en) | Preparation of adduct of nitroparaffin with vinylketone | |
JPS56128789A (en) | Preparation of organic germanium compound | |
JPS5671041A (en) | Preparation of 2-arylpropionic ester | |
JPS57108033A (en) | Oxidizing method of phenol with oxygen | |
JPS5572139A (en) | Preparation of 4-allyloxy-3,5-disubstituted-phenylacetic acid |