GB1036130A - Improvements relating to the production of acetaldehyde - Google Patents
Improvements relating to the production of acetaldehydeInfo
- Publication number
- GB1036130A GB1036130A GB35991/62A GB3599162A GB1036130A GB 1036130 A GB1036130 A GB 1036130A GB 35991/62 A GB35991/62 A GB 35991/62A GB 3599162 A GB3599162 A GB 3599162A GB 1036130 A GB1036130 A GB 1036130A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ethylene oxide
- acetaldehyde
- catalyst
- production
- improvements relating
- 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
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/56—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds
- C07C45/57—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom
- C07C45/58—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds from heterocyclic compounds with oxygen as the only heteroatom in three-membered rings
Abstract
Acetaldehyde is made by isomerizing ethylene oxide by contacting the ethylene oxide with an oxide catalyst comprising at least one of the oxides of Cr, Si, Al, Mg and W at 100-250 DEG C. in the presence of an inert liquid which boils at a temperature equal to or above the reaction temperature. The preferred catalyst is silica/alumina. Suitable inert liquids are diphenyl, terphenyl, polyphenyls, diphenyl ether, halogenated diphenyls, high boiling petroleum fractions and mixtures thereof. The reaction is suitably effected by bubbling ethylene oxide through a suspension of the catalyst in the inert liquid. The ethylene oxide may be diluted with, e.g., nitrogen.
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB35991/62A GB1036130A (en) | 1962-09-21 | 1962-09-21 | Improvements relating to the production of acetaldehyde |
BE637654A BE637654A (en) | 1962-09-21 | 1963-09-20 | Isomerization process and products obtained |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB35991/62A GB1036130A (en) | 1962-09-21 | 1962-09-21 | Improvements relating to the production of acetaldehyde |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1036130A true GB1036130A (en) | 1966-07-13 |
Family
ID=10383774
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB35991/62A Expired GB1036130A (en) | 1962-09-21 | 1962-09-21 | Improvements relating to the production of acetaldehyde |
Country Status (2)
Country | Link |
---|---|
BE (1) | BE637654A (en) |
GB (1) | GB1036130A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4925987A (en) * | 1989-04-13 | 1990-05-15 | Eastman Kodak Company | Preparation of aldehydes from unsaturated terminal epoxides |
-
1962
- 1962-09-21 GB GB35991/62A patent/GB1036130A/en not_active Expired
-
1963
- 1963-09-20 BE BE637654A patent/BE637654A/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4925987A (en) * | 1989-04-13 | 1990-05-15 | Eastman Kodak Company | Preparation of aldehydes from unsaturated terminal epoxides |
Also Published As
Publication number | Publication date |
---|---|
BE637654A (en) | 1964-03-20 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1036130A (en) | Improvements relating to the production of acetaldehyde | |
JPS4425353B1 (en) | ||
GB1049209A (en) | Improvements in and relating to the production of olefines | |
GB857504A (en) | Improvements relating to the catalytic reforming of hydrocarbons | |
GB978590A (en) | Dimerization process | |
GB1174407A (en) | Preparation of Olefins. | |
GB1081287A (en) | Process for the oxidation of 1,2,4,5-tetraalkyl benzenes | |
GB1092206A (en) | A process for the catalytic alkylation of aromatic compounds | |
GB951513A (en) | Process for the preparation of methacrolein by catalytic oxidation of isobutene | |
GB864997A (en) | Method of preparing acetaldehyde polymers | |
GB1030507A (en) | Process for the catalytic oxidation of hydrocarbons | |
GB1040308A (en) | Manufacture of 1-cyano-1, 3-butadiene | |
GB895183A (en) | Improvements in and relating to catalytic oxidation of hydrocarbons | |
AU242838B2 (en) | Stopper for vessels, especially for bottles for gaseous or sparkling liquids | |
GB951514A (en) | Improvements in or relating to the preparation of methacrolein | |
GB843424A (en) | Improvements in and relating to the polymerization of aliphatic olefins and the resulting polyolefins | |
AU6430960A (en) | Stopper for vessels, especially for bottles for gaseous or sparkling liquids | |
GB935609A (en) | Production of polycyclic aromatic hydrocarbons | |
GB1014531A (en) | Preparation of 4-methyl-1-pentene | |
GB949406A (en) | A process for preparing unsaturated aldehydes | |
GB891575A (en) | Improvements in the production of polyethylene and catalyst therefor | |
CA630014A (en) | Polymerization of olefins with metal oxide catalysts promoted by alkali metal alkyls | |
CA650200A (en) | Process for improving the stability of catalytically cracked gasoline | |
IE34210L (en) | Catalytic epoxidation of olefins. | |
GB569174A (en) | Improvements in catalytic dehydrochlorination |