JPS5553227A - Preparation of beta-phenethyl alcohol - Google Patents

Preparation of beta-phenethyl alcohol

Info

Publication number
JPS5553227A
JPS5553227A JP12519778A JP12519778A JPS5553227A JP S5553227 A JPS5553227 A JP S5553227A JP 12519778 A JP12519778 A JP 12519778A JP 12519778 A JP12519778 A JP 12519778A JP S5553227 A JPS5553227 A JP S5553227A
Authority
JP
Japan
Prior art keywords
solvent
promide
phenylethyl
under normal
beta
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
JP12519778A
Other languages
Japanese (ja)
Inventor
Kanji Katsuragawa
Keiichi Kihara
Hideo Satsuka
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.)
Tosoh Corp
Original Assignee
Toyo Soda Manufacturing Co 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 Toyo Soda Manufacturing Co Ltd filed Critical Toyo Soda Manufacturing Co Ltd
Priority to JP12519778A priority Critical patent/JPS5553227A/en
Publication of JPS5553227A publication Critical patent/JPS5553227A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE: To obtain the title compound in high purity and yield through simple procedures under normal pressures, by hydrolyzing β-phenylethyl promide in the presence of a specific solvent and a catalyst in an aqueous alkali.
CONSTITUTION: One part by wt. of with β-phenylethyl promide is hydrolyzed with an ankali salt, e.g. sodium or potassium corbonate, and water in the presence of a formate or γ-hydroxydutyrate in 0.3 part by wt. or more, preferably 0.5W10 parts by wt., of a polyethylene glycol, e.g. diethylene, thriethylene, or tetraethylene glycol as a solvent at 100W150°C, preferably 110W140°C, under normal pressures. The formed alkali metal bromide is separated by filtration, and the high-purity objective compound is obtained by distilling off a high-boiling solvent.
COPYRIGHT: (C)1980,JPO&Japio
JP12519778A 1978-10-13 1978-10-13 Preparation of beta-phenethyl alcohol Pending JPS5553227A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12519778A JPS5553227A (en) 1978-10-13 1978-10-13 Preparation of beta-phenethyl alcohol

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12519778A JPS5553227A (en) 1978-10-13 1978-10-13 Preparation of beta-phenethyl alcohol

Publications (1)

Publication Number Publication Date
JPS5553227A true JPS5553227A (en) 1980-04-18

Family

ID=14904313

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12519778A Pending JPS5553227A (en) 1978-10-13 1978-10-13 Preparation of beta-phenethyl alcohol

Country Status (1)

Country Link
JP (1) JPS5553227A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007059169A (en) * 2005-08-24 2007-03-08 Matsushita Electric Ind Co Ltd Dial rotation transmission structure

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007059169A (en) * 2005-08-24 2007-03-08 Matsushita Electric Ind Co Ltd Dial rotation transmission structure

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