JPS5490130A - Preparation of styrene glycol acetate and styrene oxide - Google Patents

Preparation of styrene glycol acetate and styrene oxide

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Publication number
JPS5490130A
JPS5490130A JP15602877A JP15602877A JPS5490130A JP S5490130 A JPS5490130 A JP S5490130A JP 15602877 A JP15602877 A JP 15602877A JP 15602877 A JP15602877 A JP 15602877A JP S5490130 A JPS5490130 A JP S5490130A
Authority
JP
Japan
Prior art keywords
styrene
compound
halide
preparation
glycol acetate
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
JP15602877A
Other languages
Japanese (ja)
Inventor
Tsuneo Ikawa
Shoichi Yamashita
Atsuo Murata
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.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
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 Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP15602877A priority Critical patent/JPS5490130A/en
Publication of JPS5490130A publication Critical patent/JPS5490130A/en
Pending legal-status Critical Current

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

Abstract

PURPOSE: To obtain the title compounds, useful as a starting material of styrene glycol and an intermediate of phenylacetic acid, in high yield and simultaneously, by the reaction of styrene with acetic acid and 02 using a Mn compound and a halogen compound as catalysts.
CONSTITUTION: Styrene is subjected to oxyacetoxylation with acetic acid and 02 at 50-150°C in the prsence of a Mn compound, e.g. KMnO4, and a halide, e.g. KI, to afford styrene glycol acetate and styrene oxide. The "Mn compound" is any Mn compound with any valence; the "halide" is any halide that can supply halogen ions. The molar ratio of Mn compound: halide is pref. 1:1W1:10. The larger the molar ratio is and the longer the reaction is, the more styrene glycol is formed. The yield of styrene glycol also depends upon the sort of the Mn compound.
USE: Intermediate of β-phenylethyl alcohol.
COPYRIGHT: (C)1979,JPO&Japio
JP15602877A 1977-12-24 1977-12-24 Preparation of styrene glycol acetate and styrene oxide Pending JPS5490130A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15602877A JPS5490130A (en) 1977-12-24 1977-12-24 Preparation of styrene glycol acetate and styrene oxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15602877A JPS5490130A (en) 1977-12-24 1977-12-24 Preparation of styrene glycol acetate and styrene oxide

Publications (1)

Publication Number Publication Date
JPS5490130A true JPS5490130A (en) 1979-07-17

Family

ID=15618724

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15602877A Pending JPS5490130A (en) 1977-12-24 1977-12-24 Preparation of styrene glycol acetate and styrene oxide

Country Status (1)

Country Link
JP (1) JPS5490130A (en)

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