GB587534A - Manufacture of esters of tertiaryamino polyhydricalcohols - Google Patents

Manufacture of esters of tertiaryamino polyhydricalcohols

Info

Publication number
GB587534A
GB587534A GB511544A GB511544A GB587534A GB 587534 A GB587534 A GB 587534A GB 511544 A GB511544 A GB 511544A GB 511544 A GB511544 A GB 511544A GB 587534 A GB587534 A GB 587534A
Authority
GB
United Kingdom
Prior art keywords
ester
alcohol
tertiaryaminopolyhydric
esters
triethanolamine
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
GB511544A
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.)
Lankro Chemicals Ltd
Original Assignee
Lankro Chemicals 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 Lankro Chemicals Ltd filed Critical Lankro Chemicals Ltd
Priority to GB511544A priority Critical patent/GB587534A/en
Publication of GB587534A publication Critical patent/GB587534A/en
Expired legal-status Critical Current

Links

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Esters of tertiaryaminopolyhydric alcohols are prepared by reacting a tertiaryaminopolyhydric alcohol with an ester of a mono or polyhydric alcohol with a straight chain aliphatic carboxylic acid having at least eight carbon atoms, in the presence of an alkali metal alkoxide catalyst. The displaced alcohol may be removed by volatilization if desired, under vacuum. In the examples: (1) ethyl oleate is added to sodium dissolved in triethanolamine and the mixture heated. A mutual solvent such as triethanolaminemonooleic ester may be added; (2) sodium dissolved in triethanolamine is heated with dry castor oil to give triethanolaminemonoricinoleic ester and glycerolmonoricinolein. Other tertiary amino polyhydric alcohols which may be employed are methyldiethanolamine, triisopropanolamine, phenyldiethanolamine and N-tertiary-dihydroxypropylamine. According to the Provisional Specification any carboxylic ester may be used, e.g. methyl acetate, dibutyl phthalate, dimethyl adipate and methyl benzoate.
GB511544A 1944-03-20 1944-03-20 Manufacture of esters of tertiaryamino polyhydricalcohols Expired GB587534A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB511544A GB587534A (en) 1944-03-20 1944-03-20 Manufacture of esters of tertiaryamino polyhydricalcohols

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB511544A GB587534A (en) 1944-03-20 1944-03-20 Manufacture of esters of tertiaryamino polyhydricalcohols

Publications (1)

Publication Number Publication Date
GB587534A true GB587534A (en) 1947-04-29

Family

ID=9789987

Family Applications (1)

Application Number Title Priority Date Filing Date
GB511544A Expired GB587534A (en) 1944-03-20 1944-03-20 Manufacture of esters of tertiaryamino polyhydricalcohols

Country Status (1)

Country Link
GB (1) GB587534A (en)

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