GB523635A - Improvements in or relating to the manufacture of unsaturated aliphatic compounds - Google Patents

Improvements in or relating to the manufacture of unsaturated aliphatic compounds

Info

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
Application number
GB946/39A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Acordis UK Ltd
Original Assignee
British Celanese Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by British Celanese Ltd filed Critical British Celanese Ltd
Publication of GB523635A publication Critical patent/GB523635A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/52Esters 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.
GB946/39A 1938-01-11 1939-01-11 Improvements in or relating to the manufacture of unsaturated aliphatic compounds Expired GB523635A (en)

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)

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