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GB616740A - Process for the manufacture of iso-phorone and related products - Google Patents

Process for the manufacture of iso-phorone and related products

Info

Publication number
GB616740A
GB616740A GB27225/46A GB2722546A GB616740A GB 616740 A GB616740 A GB 616740A GB 27225/46 A GB27225/46 A GB 27225/46A GB 2722546 A GB2722546 A GB 2722546A GB 616740 A GB616740 A GB 616740A
Authority
GB
United Kingdom
Prior art keywords
ketone
hydroxide solution
concentration
aqueous alkali
mixture
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
GB27225/46A
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.)
HUGH CAMPBELL HIGHET
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
HUGH CAMPBELL HIGHET
Distillers Co Yeast Ltd
Distillers Co 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 HUGH CAMPBELL HIGHET, Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical HUGH CAMPBELL HIGHET
Publication of GB616740A publication Critical patent/GB616740A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/68Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C45/72Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
    • C07C45/74Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups combined with dehydration

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Isophorone and homoisophorones are made by a process which comprises subjecting a saturated ketone of 3-5 carbon atoms and an aqueous alkali metal hydroxide solution, of such a concentration that the ketone is at least partially soluble therein, but which does not exceed 15 per cent by weight with respect to the hydroxide, to a temperature within the range between 150 DEG C. and the critical temperature of the ketone, whilst maintaining sufficient pressure in the reaction zone to maintain the contents in said zone substantially in the liquid phase. The mixture of ketone and aqueous alkali hydroxide solution may be one- or two-phase according to proportions and concentration. For a continuous process, a single-phase mixture is preferred. Examples describe the reaction of acetone and sodium hydroxide solution. Specification 583,863 is referred to.
GB27225/46A 1946-09-10 1946-09-10 Process for the manufacture of iso-phorone and related products Expired GB616740A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB269503X 1946-09-10
GB280847X 1947-08-28

Publications (1)

Publication Number Publication Date
GB616740A true GB616740A (en) 1949-01-26

Family

ID=26258530

Family Applications (1)

Application Number Title Priority Date Filing Date
GB27225/46A Expired GB616740A (en) 1946-09-10 1946-09-10 Process for the manufacture of iso-phorone and related products

Country Status (3)

Country Link
CH (1) CH269503A (en)
FR (1) FR953100A (en)
GB (1) GB616740A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1058047B (en) * 1953-12-24 1959-05-27 Derives De L Acetylene Soc Ind Process for the preparation of mesityl oxide or its homologues
DE1095818B (en) * 1958-09-15 1960-12-29 Bergwerksgesellschaft Hibernia Process for the production of isophorone

Also Published As

Publication number Publication date
CH269503A (en) 1950-07-15
FR953100A (en) 1949-11-30

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