GB523635A - Improvements in or relating to the manufacture of unsaturated aliphatic compounds - Google Patents
Improvements in or relating to the manufacture of unsaturated aliphatic compoundsInfo
- Publication number
- GB523635A GB523635A GB946/39A GB94639A GB523635A GB 523635 A GB523635 A GB 523635A GB 946/39 A GB946/39 A GB 946/39A GB 94639 A GB94639 A GB 94639A GB 523635 A GB523635 A GB 523635A
- Authority
- GB
- United Kingdom
- Prior art keywords
- ester
- methyl
- alcohol
- effected
- alkali
- 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
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/52—Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
523,635. Esters; synthetic resins. BRITISH CELANESE, Ltd. Jan. 11, 1939, No. 946. Convention date, Jan. 11, 1938. [Class 2 (iii)] Allyl alcohols are converted into polymerizable alkyl esters of unsaturated acids by oxidizing the alcohol to the corresponding unsaturated aldehyde, treating the aldehyde with a concentrated alkali solution to form an alkali salt of the corresponding unsaturated acid, and converting the alkali salt into an ester by treatment with an alkyl ester of an inorganic acid. The alcohols treated include methyl- and ethyl-allyl alcohols, crotonyl alcohol and methyl-crotonyl alcohol, and the alkyl components of the ester may be methyl, ethyl, propyl or butyl. The oxidation is preferably effected with free oxygen in the vapour phase. The alkali treatment may be effected in aqueous or alcoholic solution or sodium or potassium hydroxide. The products may be polymerized to form synthetic resins, and as an aid to the prevention of the formation of bubbles during polymerization, a partially polymerized product may be first formed and mixed in finely divided form with a further quantity of the monomeric ester before the final polymerization and shaping are effected. In an example, methallyl alcohol is converted through methacrolein and sodium methacrylate to methyl methacrylate.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US523635XA | 1938-01-11 | 1938-01-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB523635A true GB523635A (en) | 1940-07-18 |
Family
ID=21977129
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB946/39A Expired GB523635A (en) | 1938-01-11 | 1939-01-11 | Improvements in or relating to the manufacture of unsaturated aliphatic compounds |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB523635A (en) |
-
1939
- 1939-01-11 GB GB946/39A patent/GB523635A/en not_active Expired
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