METHOD OF DIACETONE-L-SORBOSE SYNTHESIS
FIELD: chemical technology, production of vitamins. SUBSTANCE: method involves acetonation of L-sorbose in the presence of catalyst - 24% oleum (or equivalent amount of concentrated sulfuric acid) and dehydrating agent - zeolite NaA. Acetonation components were taken at ratio, mas. p. p.: L-sorbose...
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creator | LOBANOVA A.A PANKRATOVA G.A IL'JASOV S.G |
description | FIELD: chemical technology, production of vitamins. SUBSTANCE: method involves acetonation of L-sorbose in the presence of catalyst - 24% oleum (or equivalent amount of concentrated sulfuric acid) and dehydrating agent - zeolite NaA. Acetonation components were taken at ratio, mas. p. p.: L-sorbose : oleum : acetone = 1:(0.01-0.022):(13-16). Reaction is carried out at acetone boiling point for 4 h, then solution is cooled to (-10)-(-15) C, kept for 1 h and neutralized with alkali an aqueous solution to weak alkaline reaction (pH = 8-9). Diacetone-L-sorbose is isolated by extraction with chloroform followed by solvent distillation off or extraction with toluene followed by its distillation off. Product is used for synthesis of ascorbic acid. EFFECT: increased yield of product, decreased amount of sodium salt formed. 2 tblt |
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SUBSTANCE: method involves acetonation of L-sorbose in the presence of catalyst - 24% oleum (or equivalent amount of concentrated sulfuric acid) and dehydrating agent - zeolite NaA. Acetonation components were taken at ratio, mas. p. p.: L-sorbose : oleum : acetone = 1:(0.01-0.022):(13-16). Reaction is carried out at acetone boiling point for 4 h, then solution is cooled to (-10)-(-15) C, kept for 1 h and neutralized with alkali an aqueous solution to weak alkaline reaction (pH = 8-9). Diacetone-L-sorbose is isolated by extraction with chloroform followed by solvent distillation off or extraction with toluene followed by its distillation off. Product is used for synthesis of ascorbic acid. 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EFFECT: increased yield of product, decreased amount of sodium salt formed. 2 tblt</description><subject>CHEMISTRY</subject><subject>DERIVATIVES THEREOF</subject><subject>METALLURGY</subject><subject>NUCLEIC ACIDS</subject><subject>NUCLEOSIDES</subject><subject>NUCLEOTIDES</subject><subject>ORGANIC CHEMISTRY</subject><subject>SUGARS</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1998</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZFD3dQ3x8HdR8HdTcPF0dHYN8fdz1fXRDfYPcvIPdlUIjvQL8XAN9gzmYWBNS8wpTuWF0twMCm6uIc4euqkF-fGpxQWJyal5qSXxQaFGhgaGRpYGzobGRCgBAKSnI4s</recordid><startdate>19980110</startdate><enddate>19980110</enddate><creator>LOBANOVA A.A</creator><creator>PANKRATOVA G.A</creator><creator>IL'JASOV S.G</creator><scope>EVB</scope></search><sort><creationdate>19980110</creationdate><title>METHOD OF DIACETONE-L-SORBOSE SYNTHESIS</title><author>LOBANOVA A.A ; PANKRATOVA G.A ; IL'JASOV S.G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_RU2101290C13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1998</creationdate><topic>CHEMISTRY</topic><topic>DERIVATIVES THEREOF</topic><topic>METALLURGY</topic><topic>NUCLEIC ACIDS</topic><topic>NUCLEOSIDES</topic><topic>NUCLEOTIDES</topic><topic>ORGANIC CHEMISTRY</topic><topic>SUGARS</topic><toplevel>online_resources</toplevel><creatorcontrib>LOBANOVA A.A</creatorcontrib><creatorcontrib>PANKRATOVA G.A</creatorcontrib><creatorcontrib>IL'JASOV S.G</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>LOBANOVA A.A</au><au>PANKRATOVA G.A</au><au>IL'JASOV S.G</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>METHOD OF DIACETONE-L-SORBOSE SYNTHESIS</title><date>1998-01-10</date><risdate>1998</risdate><abstract>FIELD: chemical technology, production of vitamins. SUBSTANCE: method involves acetonation of L-sorbose in the presence of catalyst - 24% oleum (or equivalent amount of concentrated sulfuric acid) and dehydrating agent - zeolite NaA. Acetonation components were taken at ratio, mas. p. p.: L-sorbose : oleum : acetone = 1:(0.01-0.022):(13-16). Reaction is carried out at acetone boiling point for 4 h, then solution is cooled to (-10)-(-15) C, kept for 1 h and neutralized with alkali an aqueous solution to weak alkaline reaction (pH = 8-9). Diacetone-L-sorbose is isolated by extraction with chloroform followed by solvent distillation off or extraction with toluene followed by its distillation off. Product is used for synthesis of ascorbic acid. EFFECT: increased yield of product, decreased amount of sodium salt formed. 2 tblt</abstract><edition>6</edition><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY DERIVATIVES THEREOF METALLURGY NUCLEIC ACIDS NUCLEOSIDES NUCLEOTIDES ORGANIC CHEMISTRY SUGARS |
title | METHOD OF DIACETONE-L-SORBOSE SYNTHESIS |
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