GB915798A - Improvements in the production of dicarbonyl compounds - Google Patents
Improvements in the production of dicarbonyl compoundsInfo
- Publication number
- GB915798A GB915798A GB1177661A GB1177661A GB915798A GB 915798 A GB915798 A GB 915798A GB 1177661 A GB1177661 A GB 1177661A GB 1177661 A GB1177661 A GB 1177661A GB 915798 A GB915798 A GB 915798A
- Authority
- GB
- United Kingdom
- Prior art keywords
- selenium
- production
- ketone
- contain
- cyclohexanone
- 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
- 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
- C07C51/31—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation of cyclic compounds with ring-splitting
- C07C51/313—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation of cyclic compounds with ring-splitting with molecular oxygen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/40—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation with ozone; by ozonolysis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/04—Saturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/12—Ketones containing more than one keto group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/385—Saturated compounds containing a keto group being part of a ring
- C07C49/395—Saturated compounds containing a keto group being part of a ring of a five-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/385—Saturated compounds containing a keto group being part of a ring
- C07C49/403—Saturated compounds containing a keto group being part of a ring of a six-membered ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/34—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with ozone; by hydrolysis of ozonides
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
Alpha dicarbonyl compounds are obtained by oxidising, in the liquid phase, carbonyl compounds, which contain a methylene group adjacent to the carbonyl group, with ozone in presence of a selenium catalyst e.g. selenium dioxide or elemental selenium. The reaction mixture may contain an inert solvent or diluent e.g. water, and the oxidation may be effected at -5 DEG to +90 DEG C. Carbonyl compounds which may be used in the process include methyl ethyl ketone, diethyl ketone, methyl benzyl ketone, cyclopentanone, and methyl cyclohexanone. Aldehydes of the type -CH2-CHO may also be used. Examples describe the production of diacetyl from methyl ethyl ketone, and of cyclohexane-1,2-dione from cyclohexanone, (adipic acid being also obtained).
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1177661A GB915798A (en) | 1961-03-30 | 1961-03-30 | Improvements in the production of dicarbonyl compounds |
FR858396A FR1287734A (en) | 1961-03-30 | 1961-04-11 | Improvements to processes for the production of dicarbonyl compounds |
US139058A US3153066A (en) | 1961-03-30 | 1961-09-19 | Process for dicarbonyl compounds |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB1177661A GB915798A (en) | 1961-03-30 | 1961-03-30 | Improvements in the production of dicarbonyl compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB915798A true GB915798A (en) | 1963-01-16 |
Family
ID=9992490
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB1177661A Expired GB915798A (en) | 1961-03-30 | 1961-03-30 | Improvements in the production of dicarbonyl compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB915798A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102381931A (en) * | 2010-08-31 | 2012-03-21 | 中国石油化工股份有限公司 | Method for oxidizing cyclohexanone |
CN104591985A (en) * | 2015-01-08 | 2015-05-06 | 河南师范大学 | Method for synthesizing diacetyl through catalytic oxidation of butanone by using PEG/NOx |
-
1961
- 1961-03-30 GB GB1177661A patent/GB915798A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102381931A (en) * | 2010-08-31 | 2012-03-21 | 中国石油化工股份有限公司 | Method for oxidizing cyclohexanone |
CN102381931B (en) * | 2010-08-31 | 2013-12-25 | 中国石油化工股份有限公司 | Method for oxidizing cyclohexanone |
CN104591985A (en) * | 2015-01-08 | 2015-05-06 | 河南师范大学 | Method for synthesizing diacetyl through catalytic oxidation of butanone by using PEG/NOx |
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