JPS56158734A - Preparation of p-n-alkylbenzoic acid - Google Patents

Preparation of p-n-alkylbenzoic acid

Info

Publication number
JPS56158734A
JPS56158734A JP6181580A JP6181580A JPS56158734A JP S56158734 A JPS56158734 A JP S56158734A JP 6181580 A JP6181580 A JP 6181580A JP 6181580 A JP6181580 A JP 6181580A JP S56158734 A JPS56158734 A JP S56158734A
Authority
JP
Japan
Prior art keywords
ketone
expressed
formula
acid
alkyl
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.)
Pending
Application number
JP6181580A
Other languages
Japanese (ja)
Inventor
Kazuya Nagaoka
Koji Kusabe
Shuichi Nakatani
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.)
Kawasaki Kasei Chemicals Ltd
Original Assignee
Kawasaki Kasei 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 Kawasaki Kasei Chemicals Ltd filed Critical Kawasaki Kasei Chemicals Ltd
Priority to JP6181580A priority Critical patent/JPS56158734A/en
Publication of JPS56158734A publication Critical patent/JPS56158734A/en
Pending legal-status Critical Current

Links

Landscapes

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

Abstract

PURPOSE: To obtain the titled compound of high purity useful as a liquid crystal material, etc., readily in a simple operation and inexpensively, by the reaction of p-formylbenzoic acid with a ketone in the presence of a basis catalyst, and the reduction of the resultant product.
CONSTITUTION: p-Formylbenzoic acid expressed by formula I is reacted with a methyl n-alkyl ketone expressed by formula II (R is n-alkyl) in the presence of a basic catalyst, preferably by the addition of water in an amount equal to that of the ketone, at 0W50°C. The resultant reaction mixture containing an intermediate compound expressed by formula III is acidified with a mineral acid, e.g. hydrochloric acid, and the intermediate compound expressed by formula III is dehydrated, preferably under heating, to produce an unsaturated ketone expressed by formula IV. Then the vinylene group of the unsaturated ketone is hydrogenated into an ethylene group to give a saturated ketone, which is then reduced to afford the aimed compound.
EFFECT: An expensive reagent, e.g., AlCl3, is not required and the waste water is treated simply.
COPYRIGHT: (C)1981,JPO&Japio
JP6181580A 1980-05-12 1980-05-12 Preparation of p-n-alkylbenzoic acid Pending JPS56158734A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6181580A JPS56158734A (en) 1980-05-12 1980-05-12 Preparation of p-n-alkylbenzoic acid

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6181580A JPS56158734A (en) 1980-05-12 1980-05-12 Preparation of p-n-alkylbenzoic acid

Publications (1)

Publication Number Publication Date
JPS56158734A true JPS56158734A (en) 1981-12-07

Family

ID=13181950

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6181580A Pending JPS56158734A (en) 1980-05-12 1980-05-12 Preparation of p-n-alkylbenzoic acid

Country Status (1)

Country Link
JP (1) JPS56158734A (en)

Similar Documents

Publication Publication Date Title
JPS56158734A (en) Preparation of p-n-alkylbenzoic acid
JPS57128653A (en) Preparation of alpha-oxyisobutyric acid
JPS57108025A (en) Preparation of secondary alcohol
JPS55143919A (en) Preparation of tertiary alcohol
JPS5655345A (en) Preparation of 2-pentenoate ester
JPS54128507A (en) Preparation of ethylene glycol
JPS5610135A (en) Preparation of di-n-propylmalonic acid
JPS54160324A (en) Purification of m-dinitrobenzene
JPS56120627A (en) Selective reduction of compound having acetylenic unsaturated bond
JPS5697245A (en) Preparation of carboxylic acid
JPS5427507A (en) Preparation of tertiary butyl alcohol
JPS57102882A (en) Preparation of furancarbonyl chloride
JPS56103145A (en) Preparation of amide compound containing vinyl group
JPS56166142A (en) Preparation of m-phenoxybenzaldehyde
JPS5562050A (en) Preparation of substituted phenylacetohydroxamic acid
JPS5762228A (en) Preparation of 2,4-diphenyl-4-methyl-pentene
JPS57156439A (en) Continuous preparation of monochloroacetic acid ester
JPS5268155A (en) Preparation of 4'-alkyl-4-biphenylcarbonitrile
JPS54163504A (en) Production of conjugated diene compound
JPS57206636A (en) Preparation of 3,3-dimethylbutyric acid
JPS54138507A (en) Preparation of diisobutene
JPS57183730A (en) Liquid crystal compound
JPS5416457A (en) Synthesis of biphenyl derivatives
JPS5716833A (en) Preparation of substituted acetic ester
JPS54148773A (en) Preparation of phthalide