GB764053A - Improvements in or relating to preparation of bis (chloromethyl) oxacyclobutane - Google Patents

Improvements in or relating to preparation of bis (chloromethyl) oxacyclobutane

Info

Publication number
GB764053A
GB764053A GB2411/55A GB241155A GB764053A GB 764053 A GB764053 A GB 764053A GB 2411/55 A GB2411/55 A GB 2411/55A GB 241155 A GB241155 A GB 241155A GB 764053 A GB764053 A GB 764053A
Authority
GB
United Kingdom
Prior art keywords
hydroxide
oxacyclobutane
chloromethyl
bis
trichloride
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.)
Expired
Application number
GB2411/55A
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.)
Hercules Powder Co
Original Assignee
Hercules Powder Co
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 Hercules Powder Co filed Critical Hercules Powder Co
Publication of GB764053A publication Critical patent/GB764053A/en
Expired legal-status Critical Current

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

Abstract

A process of preparing 3,3-bis (chloromethyl) oxacyclobutane comprises reacting a dispersion of pentaerythritol trichloride or an ester thereof in aqueous medium with an alkali metal hydroxide or an alkaline earth metal hydroxide at a temperature of 90 DEG to 170 DEG C., the concentration of dissolved hydroxide in the aqueous phase not exceeding 70 per cent. The ester may be pentaerythritol trichloride monoacetate, propionate or hydrogen sulphate. The hydroxide may be sodium hydroxide, potassium hydroxide, calcium hydroxide or barium hydroxide. Wetting or dispersing agents, such as sodium stearate, alkylarylsulphonates and nonylphenol ethylene oxide adduct, may be present. The temperature is preferably from 100 DEG to 130 DEG C., and the concentration of dissolved hydroxide is preferably from 10 to 50 per cent. Examples of the process are given.
GB2411/55A 1954-06-01 1955-01-26 Improvements in or relating to preparation of bis (chloromethyl) oxacyclobutane Expired GB764053A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US764053XA 1954-06-01 1954-06-01

Publications (1)

Publication Number Publication Date
GB764053A true GB764053A (en) 1956-12-19

Family

ID=22131816

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2411/55A Expired GB764053A (en) 1954-06-01 1955-01-26 Improvements in or relating to preparation of bis (chloromethyl) oxacyclobutane

Country Status (1)

Country Link
GB (1) GB764053A (en)

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