PRODUCTION OF BIS-(BETA-HYDROXYALKYL)-SULFONES
1,157,710. Production of bis-(#-hydroxyalkyl)- sulfones. BADISCHE ANILIN- & SODAFABKIK A.G. 25 Nov., 1966 [27 Nov., 1965], No. 52869/66. Heading C2C. Bis-(#-hydroxyalkyl)-sulfones are prepared by reacting salts of hydroxy-methanesulphinic acid with 1,2-epoxides having from 2C to 20C in inert sol...
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description | 1,157,710. Production of bis-(#-hydroxyalkyl)- sulfones. BADISCHE ANILIN- & SODAFABKIK A.G. 25 Nov., 1966 [27 Nov., 1965], No. 52869/66. Heading C2C. Bis-(#-hydroxyalkyl)-sulfones are prepared by reacting salts of hydroxy-methanesulphinic acid with 1,2-epoxides having from 2C to 20C in inert solvents at temperatures of 0-100 C., pH of 4 to 10 and with the addition of an acid. Preferably, the sodium, potassium or zinc salts are used, with water as the solvent. The acids include H 2 SO 4 , HC1, H 3 PO 4 , HCO 2 H or CH 3 CO 2 H. Hydroxymethanesulphinic acid salts are made by reacting a bisulphite, e.g. sodium metabisulphite with formaldehyde and reducing for example with sodium amalgam. |
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Bis-(#-hydroxyalkyl)-sulfones are prepared by reacting salts of hydroxy-methanesulphinic acid with 1,2-epoxides having from 2C to 20C in inert solvents at temperatures of 0-100 C., pH of 4 to 10 and with the addition of an acid. Preferably, the sodium, potassium or zinc salts are used, with water as the solvent. The acids include H 2 SO 4 , HC1, H 3 PO 4 , HCO 2 H or CH 3 CO 2 H. 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Production of bis-(#-hydroxyalkyl)- sulfones. BADISCHE ANILIN- & SODAFABKIK A.G. 25 Nov., 1966 [27 Nov., 1965], No. 52869/66. Heading C2C. Bis-(#-hydroxyalkyl)-sulfones are prepared by reacting salts of hydroxy-methanesulphinic acid with 1,2-epoxides having from 2C to 20C in inert solvents at temperatures of 0-100 C., pH of 4 to 10 and with the addition of an acid. Preferably, the sodium, potassium or zinc salts are used, with water as the solvent. The acids include H 2 SO 4 , HC1, H 3 PO 4 , HCO 2 H or CH 3 CO 2 H. Hydroxymethanesulphinic acid salts are made by reacting a bisulphite, e.g. sodium metabisulphite with formaldehyde and reducing for example with sodium amalgam.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1969</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZNALCPJ3CXUO8fT3U_B3U3DyDNbVcHINcdT1iHQJ8o-IdPTxjvTR1A0O9XHz93MN5mFgTUvMKU7lhdLcDPJuriHOHrqpBfnxqcUFicmpeakl8aHBxiamZgaGZo7GhFUAAGeDJUI</recordid><startdate>19690715</startdate><enddate>19690715</enddate><creator>HARRY DISTLER</creator><scope>EVB</scope></search><sort><creationdate>19690715</creationdate><title>PRODUCTION OF BIS-(BETA-HYDROXYALKYL)-SULFONES</title><author>HARRY DISTLER</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_US3456016A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1969</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>HARRY DISTLER</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>HARRY DISTLER</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>PRODUCTION OF BIS-(BETA-HYDROXYALKYL)-SULFONES</title><date>1969-07-15</date><risdate>1969</risdate><abstract>1,157,710. Production of bis-(#-hydroxyalkyl)- sulfones. BADISCHE ANILIN- & SODAFABKIK A.G. 25 Nov., 1966 [27 Nov., 1965], No. 52869/66. Heading C2C. Bis-(#-hydroxyalkyl)-sulfones are prepared by reacting salts of hydroxy-methanesulphinic acid with 1,2-epoxides having from 2C to 20C in inert solvents at temperatures of 0-100 C., pH of 4 to 10 and with the addition of an acid. Preferably, the sodium, potassium or zinc salts are used, with water as the solvent. The acids include H 2 SO 4 , HC1, H 3 PO 4 , HCO 2 H or CH 3 CO 2 H. Hydroxymethanesulphinic acid salts are made by reacting a bisulphite, e.g. sodium metabisulphite with formaldehyde and reducing for example with sodium amalgam.</abstract><oa>free_for_read</oa></addata></record> |
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title | PRODUCTION OF BIS-(BETA-HYDROXYALKYL)-SULFONES |
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