GB830813A - Production of triacetone dialcohol - Google Patents

Production of triacetone dialcohol

Info

Publication number
GB830813A
GB830813A GB3717257A GB3717257A GB830813A GB 830813 A GB830813 A GB 830813A GB 3717257 A GB3717257 A GB 3717257A GB 3717257 A GB3717257 A GB 3717257A GB 830813 A GB830813 A GB 830813A
Authority
GB
United Kingdom
Prior art keywords
acetone
triacetone
dialcohol
triacetone dialcohol
production
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
GB3717257A
Inventor
Ernest Cecil Craven
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.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
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 Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB3717257A priority Critical patent/GB830813A/en
Publication of GB830813A publication Critical patent/GB830813A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/04Saturated compounds containing keto groups bound to acyclic carbon atoms
    • C07C49/17Saturated compounds containing keto groups bound to acyclic carbon atoms containing hydroxy groups

Landscapes

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

Abstract

Triacetone dialcohol is prepared along with diacetone alcohol by mixing acetone with an alkali metal hydroxide in solution in a C1-4 alkanol at -30 DEG to +15 DEG C. Preferably 0.002 to 0.02 grams of alkali metal hydroxide are used per 100 ml. of acetone. The temperature preferably does not exceed 0 DEG C. Acetone containing up to 0.5% by volume of water may be used. The triacetone dialcohol may be recovered by, for example, neutralizing the alkali with acid, distilling the acetone at atmospheric pressure, filtering off the salt formed in the neutralization, and then removing diacetone alcohol at reduced pressure leaving the triacetone dialcohol as the residue.
GB3717257A 1957-11-28 1957-11-28 Production of triacetone dialcohol Expired GB830813A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3717257A GB830813A (en) 1957-11-28 1957-11-28 Production of triacetone dialcohol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3717257A GB830813A (en) 1957-11-28 1957-11-28 Production of triacetone dialcohol

Publications (1)

Publication Number Publication Date
GB830813A true GB830813A (en) 1960-03-23

Family

ID=10394358

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3717257A Expired GB830813A (en) 1957-11-28 1957-11-28 Production of triacetone dialcohol

Country Status (1)

Country Link
GB (1) GB830813A (en)

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