GB599365A - Improvements in the production of substituted butanols - Google Patents

Improvements in the production of substituted butanols

Info

Publication number
GB599365A
GB599365A GB23973/45A GB2397345A GB599365A GB 599365 A GB599365 A GB 599365A GB 23973/45 A GB23973/45 A GB 23973/45A GB 2397345 A GB2397345 A GB 2397345A GB 599365 A GB599365 A GB 599365A
Authority
GB
United Kingdom
Prior art keywords
tetrahydrophenyl
cyclohexyl
beta
product
methyl ketone
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
GB23973/45A
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.)
Acordis UK Ltd
Original Assignee
British Celanese 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 British Celanese Ltd filed Critical British Celanese Ltd
Publication of GB599365A publication Critical patent/GB599365A/en
Expired legal-status Critical Current

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  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

1-Cyclohexyl-butanol-3 is made by hydrogenating beta - (1, 2, 5, 6 - tetrahydrophenyl) - vinyl methyl ketone in the presence of a nickel catalyst, for example at a temperature of 20 to 100 DEG C. and under a pressure up to 2,000 lbs. per square inch. The product may then be esterified or etherified. The beta-(1, 2, 5, 6-tetrahydrophenyl)- vinyl methyl ketone may be prepared by reacting acrolein with 1, 3-butadiene and condensing the 1, 2, 5, 6-tetrahydrobenzaldehyde so produced with acetone in the presence of a strong base. In examples: (1) beta - (1, 2, 5, 6 - tetrahydrophenyl) - vinyl methyl ketone is hydrogenated in solution in ethyl alcohol in the presence of Raney nickel; (2) the product of (1) is esterified by means of propionic anhydride to yield 1 - cyclohexyl - 3 - propionoxy - butane; (3) the product of (1) is etherified by dissolving in ether and adding sodium, and then adding dimethyl sulphate to give 1-cyclohexyl-3-methoxy-butane. Other esters and ethers mentioned are the esters of butyric, acrylic. succinic, phthalic and hexahydrobenzoic acids, and the ethers of ethyl, propyl, butyl, lauryl and benzyl alcohols, phenols, and the polyhydric alcohols such as ethylene glycol, propylene glycol and glycerol.
GB23973/45A 1944-09-21 1945-09-17 Improvements in the production of substituted butanols Expired GB599365A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US599365XA 1944-09-21 1944-09-21

Publications (1)

Publication Number Publication Date
GB599365A true GB599365A (en) 1948-03-10

Family

ID=22026256

Family Applications (1)

Application Number Title Priority Date Filing Date
GB23973/45A Expired GB599365A (en) 1944-09-21 1945-09-17 Improvements in the production of substituted butanols

Country Status (1)

Country Link
GB (1) GB599365A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3183151A (en) * 1961-01-06 1965-05-11 Kuhlmann Ets Treatment of hypocholeresis with 1-cyclohexyl-2-methyl-1-propanol

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3183151A (en) * 1961-01-06 1965-05-11 Kuhlmann Ets Treatment of hypocholeresis with 1-cyclohexyl-2-methyl-1-propanol

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