GB918403A - Improvements in or relating to polyalcohols - Google Patents

Improvements in or relating to polyalcohols

Info

Publication number
GB918403A
GB918403A GB157961A GB157961A GB918403A GB 918403 A GB918403 A GB 918403A GB 157961 A GB157961 A GB 157961A GB 157961 A GB157961 A GB 157961A GB 918403 A GB918403 A GB 918403A
Authority
GB
United Kingdom
Prior art keywords
polyalcohols
preparation
added
dimethyl formamide
formaldehyde
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
GB157961A
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.)
REPUBLIC OF FRANCE
Original Assignee
REPUBLIC OF FRANCE
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 REPUBLIC OF FRANCE filed Critical REPUBLIC OF FRANCE
Publication of GB918403A publication Critical patent/GB918403A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/18Polyhydroxylic acyclic alcohols

Landscapes

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

Abstract

In a process for the preparation of polyalcohols by the reaction of formaldehyde and an aliphatic carbonyl compound in an aqueous alkaline solution at a pH between 4 and 7, after removal of the unreacted formaldehyde an aliphatic primary N-dialkyl-substituted amide <FORM:0918403/IV (b)/1> in which R4 represents hydrogen or an alkyl radical and R2 and R3 alkyl radicals, is added to the reaction solution which is concentrated at between 50 and 130 DEG C. to eliminate water and precipitate mineral salts, and the polyalcohol is then recovered. The preparation of trimethylol ethane, trimethylol propane, and pentaerythritol in which N-dimethyl formamide is used are exemplified and amides such as N-dimethyl acetamide, N-diethylacetamide, N-dimethyl formamide, and N-propylformamide are referred to. The synthesis solution may be preconcentrated at not more than 120 DEG C. and from 0.1 to 10 times the partial volume of the polyalcohols, of amide may be added.
GB157961A 1960-01-30 1961-01-13 Improvements in or relating to polyalcohols Expired GB918403A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR817149A FR1255983A (en) 1960-01-30 1960-01-30 Improvement in the process for preparing polyalcohols such as methylolalkanes

Publications (1)

Publication Number Publication Date
GB918403A true GB918403A (en) 1963-02-13

Family

ID=8724549

Family Applications (1)

Application Number Title Priority Date Filing Date
GB157961A Expired GB918403A (en) 1960-01-30 1961-01-13 Improvements in or relating to polyalcohols

Country Status (5)

Country Link
BE (1) BE599316A (en)
ES (1) ES264776A1 (en)
FR (1) FR1255983A (en)
GB (1) GB918403A (en)
LU (1) LU39687A1 (en)

Also Published As

Publication number Publication date
FR1255983A (en) 1961-03-17
LU39687A1 (en) 1961-03-25
BE599316A (en) 1961-05-16
ES264776A1 (en) 1961-04-16

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