GB989243A - Production of pentaerythritol and dipentaerythritol - Google Patents

Production of pentaerythritol and dipentaerythritol

Info

Publication number
GB989243A
GB989243A GB2820761A GB2820761A GB989243A GB 989243 A GB989243 A GB 989243A GB 2820761 A GB2820761 A GB 2820761A GB 2820761 A GB2820761 A GB 2820761A GB 989243 A GB989243 A GB 989243A
Authority
GB
United Kingdom
Prior art keywords
formaldehyde
dipentaerythritol
pentaerythritol
acetaldehyde
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
GB2820761A
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.)
Celanese Corp
Original Assignee
Celanese Corp
Celanese Corp of America
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 Celanese Corp, Celanese Corp of America filed Critical Celanese Corp
Publication of GB989243A publication Critical patent/GB989243A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00Ethers; Compounds having groups, groups or groups
    • C07C43/02Ethers
    • C07C43/03Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
    • C07C43/04Saturated ethers
    • C07C43/13Saturated ethers containing hydroxy or O-metal groups
    • C07C43/132Saturated ethers containing hydroxy or O-metal groups both carbon chains being substituted by hydroxy or O-metal groups

Abstract

A product containing both pentaerythritol and dipentaerythritol is obtained by reacting together formaldehyde, acetaldehyde and a base by first forming a reaction mixture in which the process is substantially complete and then adding further quantities of the reactants at such a rate that the concentrations of free aldehydes in the mixture do not increase substantially. The formaldehyde is used as an aqueous solution of 5-12% by weight concentration. Preferably the molar ratio of formaldehyde to acetaldehyde is from 4:1 to 10:1 and the base used is sodium or potassium hydroxide. The preferred temperature range for carrying out the process is 50-90 DEG C.
GB2820761A 1960-08-03 1961-08-03 Production of pentaerythritol and dipentaerythritol Expired GB989243A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US4715760A 1960-08-03 1960-08-03

Publications (1)

Publication Number Publication Date
GB989243A true GB989243A (en) 1965-04-14

Family

ID=21947369

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2820761A Expired GB989243A (en) 1960-08-03 1961-08-03 Production of pentaerythritol and dipentaerythritol

Country Status (1)

Country Link
GB (1) GB989243A (en)

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