JPS56166138A - Preparation of 4-trifluoromethyl-4'-isopropenyl-diphenyl ether - Google Patents

Preparation of 4-trifluoromethyl-4'-isopropenyl-diphenyl ether

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Publication number
JPS56166138A
JPS56166138A JP6958980A JP6958980A JPS56166138A JP S56166138 A JPS56166138 A JP S56166138A JP 6958980 A JP6958980 A JP 6958980A JP 6958980 A JP6958980 A JP 6958980A JP S56166138 A JPS56166138 A JP S56166138A
Authority
JP
Japan
Prior art keywords
compound
hydroxide
carbonate
alkaline agent
concentration
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
JP6958980A
Other languages
Japanese (ja)
Inventor
Nobukatsu Kato
Teruo Yuasa
Yoshio Morimoto
Tsutomu Takase
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.)
Mitsui Toatsu Chemicals Inc
Original Assignee
Mitsui Toatsu Chemicals Inc
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 Mitsui Toatsu Chemicals Inc filed Critical Mitsui Toatsu Chemicals Inc
Priority to JP6958980A priority Critical patent/JPS56166138A/en
Publication of JPS56166138A publication Critical patent/JPS56166138A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE: To obtain the titled substance in high yield, by reacting p-isopropenylphenol of a specific concentration with an alkali metallic hydroxide in DMSO solvent, removing the formed water, and then reacting the resultant product with p- trifluoromethylchlorobenzene.
CONSTITUTION: p-Isopropenylphenol (A) is reacted with an alkali metallic hydroxide or its mixture with its carbonate as an alkaline agent in DMSO solvent to remove the formed water, and then p-trifluoromethylchlorobenzene (B) is added and reacted at 140W170°C to give a compound of the formula. The concentration of the compound (A) in the DMSO has a great influence on the reaction efficiency, and the preferable concentration is 5W30wt%. When the hydroxide and carbonate are used together as the alkaline agent, the molar ratio of hydroxide:carbonate is 1:0.1W0.2. The molar ratio of the compound (A): the alkaline agent is 1:1.0W1.2, and that of the compound (A): the compound (B) is 1:1.5W3.0.
USE: An intermediate for agricultural chemicals and medicines.
COPYRIGHT: (C)1981,JPO&Japio
JP6958980A 1980-05-27 1980-05-27 Preparation of 4-trifluoromethyl-4'-isopropenyl-diphenyl ether Pending JPS56166138A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6958980A JPS56166138A (en) 1980-05-27 1980-05-27 Preparation of 4-trifluoromethyl-4'-isopropenyl-diphenyl ether

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6958980A JPS56166138A (en) 1980-05-27 1980-05-27 Preparation of 4-trifluoromethyl-4'-isopropenyl-diphenyl ether

Publications (1)

Publication Number Publication Date
JPS56166138A true JPS56166138A (en) 1981-12-21

Family

ID=13407158

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6958980A Pending JPS56166138A (en) 1980-05-27 1980-05-27 Preparation of 4-trifluoromethyl-4'-isopropenyl-diphenyl ether

Country Status (1)

Country Link
JP (1) JPS56166138A (en)

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