JPS5444636A - Production of tetrabromobisphenol-s - Google Patents

Production of tetrabromobisphenol-s

Info

Publication number
JPS5444636A
JPS5444636A JP11048577A JP11048577A JPS5444636A JP S5444636 A JPS5444636 A JP S5444636A JP 11048577 A JP11048577 A JP 11048577A JP 11048577 A JP11048577 A JP 11048577A JP S5444636 A JPS5444636 A JP S5444636A
Authority
JP
Japan
Prior art keywords
water
reaction
organic solvent
bisphenol
bromine
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
JP11048577A
Other languages
Japanese (ja)
Inventor
Kimihiko Sato
Isao Goto
Masaaki Ikemura
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.)
AGC Inc
Original Assignee
Asahi Glass 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 Asahi Glass Co Ltd filed Critical Asahi Glass Co Ltd
Priority to JP11048577A priority Critical patent/JPS5444636A/en
Publication of JPS5444636A publication Critical patent/JPS5444636A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE: In the bromination of bisphenol-S, a heterogeneous solvent consisting of water and an organic solvent is used as the reaction medium and hydrogen bromide evolving during the reaction is dissolved in the water to prevent troubles, thus producing titled compound useful as flame retarder by simple operations.
CONSTITUTION: In a heterogeneous mixture consisting of water and an organic solvent in a volume ratio 5W60 water to 95W40 solvent, in which the organic solvent is preferably a halogenated organic solvent that is less soluble in water such as carbon tetrachloride, the bromination of bisphenol-S of formulaIwith bromine is conducted to produce said tetrabromobisphenol-S formula II. The reaction temperature is preferably 10W80°C and the amount of bromine used in the reaction is about 4 moles per mole of the bisphenol S or a little excess. The hydrogen bromide evolving during the reaction immediately dissolves in water and does not accumulate in the organic solvent.
EFFECT: After the completion of the reaction, an aqueous hydrobromic acid is obtained and bromine is regenerated therefrom readily.
COPYRIGHT: (C)1979,JPO&Japio
JP11048577A 1977-09-16 1977-09-16 Production of tetrabromobisphenol-s Pending JPS5444636A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP11048577A JPS5444636A (en) 1977-09-16 1977-09-16 Production of tetrabromobisphenol-s

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP11048577A JPS5444636A (en) 1977-09-16 1977-09-16 Production of tetrabromobisphenol-s

Publications (1)

Publication Number Publication Date
JPS5444636A true JPS5444636A (en) 1979-04-09

Family

ID=14536917

Family Applications (1)

Application Number Title Priority Date Filing Date
JP11048577A Pending JPS5444636A (en) 1977-09-16 1977-09-16 Production of tetrabromobisphenol-s

Country Status (1)

Country Link
JP (1) JPS5444636A (en)

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