GB476387A - Improved process for electrolytic production of esters - Google Patents
Improved process for electrolytic production of estersInfo
- Publication number
- GB476387A GB476387A GB15936/36A GB1593636A GB476387A GB 476387 A GB476387 A GB 476387A GB 15936/36 A GB15936/36 A GB 15936/36A GB 1593636 A GB1593636 A GB 1593636A GB 476387 A GB476387 A GB 476387A
- Authority
- GB
- United Kingdom
- Prior art keywords
- esters
- acid
- production
- nitric
- nitric acid
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B3/00—Electrolytic production of organic compounds
- C25B3/20—Processes
- C25B3/23—Oxidation
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
476,387. Eiectrolytic production of esters. NITROGLYCERIN AKTIEBOLAGET, and OHMAN, V. June 8, 1936, No. 15936. Addition to 455,463. [Class 41] Nitric acid esters are produced by anodic oxidation of unsaturated carbon compounds other than olefinic hydrocarbons in the presence of a nitric acid and/or a nitrate. The anolyte should contain a solvent for the carbon compound such as acetic acid or acetone and a conducting salt such as calcium nitrate; the hydroxyl ion concentration is maintained below pH 4 by addition of nitric and/or acetic acid. Gaseous carbon compounds may be introduced under pressure. The anode should have a high over-voltage for oxygen and is preferably of smooth platinum. The reaction may be carried out in a substantially waterfree medium. The oxidation may be limited to production of the esters by providing in the anode compartment a liquid immiscible therewith which dissolves the ester as formed, as described in the parent Specification. Detailed examples are given for the production of nitric acid esters from vinyl bromide, allyl bromide, allyl alcohol, acrylic acid, crotonic acid (alpha), maleic acid, vinyl acetate, isoprene, butadiene, di-methyl butadiene, allene, chloroprene, phorone, cyclo-pentadiene, and pyromucic acid. Esters may also be produced from aromatic compounds having unsaturated side chains.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB15936/36A GB476387A (en) | 1936-06-08 | 1936-06-08 | Improved process for electrolytic production of esters |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB15936/36A GB476387A (en) | 1936-06-08 | 1936-06-08 | Improved process for electrolytic production of esters |
Publications (1)
Publication Number | Publication Date |
---|---|
GB476387A true GB476387A (en) | 1937-12-08 |
Family
ID=10068205
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB15936/36A Expired GB476387A (en) | 1936-06-08 | 1936-06-08 | Improved process for electrolytic production of esters |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB476387A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4193850A (en) * | 1979-04-12 | 1980-03-18 | Hoffmann-La Roche Inc. | Alkanoyloxylation of beta-ionone |
-
1936
- 1936-06-08 GB GB15936/36A patent/GB476387A/en not_active Expired
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4193850A (en) * | 1979-04-12 | 1980-03-18 | Hoffmann-La Roche Inc. | Alkanoyloxylation of beta-ionone |
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