Procedure for the alkylation of 3,4-dihydroxythiophene-2,5-dicarboxylic esters
Reaction of 3,4-dihydroxythiophene-2,5-dicarboxylic esters with alkylating agents in a polar diluent is effected in presence of a quaternary onium salt. Also claimed is the novel compound 3,4-ethylenedioxythiophene-2,5-dicarboxylic acid monohydrate. Reaction of 3,4-dihydroxythiophene-2,5-dicarboxyli...
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creator | KLAUSENER, ALEXANDER DR WINKLER, ADOLF DR SCHENKEL, RALFO DR BREMEN, JOSEF DR RAUCHSCHWALBE, GUENTER DR |
description | Reaction of 3,4-dihydroxythiophene-2,5-dicarboxylic esters with alkylating agents in a polar diluent is effected in presence of a quaternary onium salt. Also claimed is the novel compound 3,4-ethylenedioxythiophene-2,5-dicarboxylic acid monohydrate. Reaction of 3,4-dihydroxythiophene-2,5-dicarboxylic esters of formula (I) with alkylating agents in a polar diluent is effected in presence of a quaternary onium salt of formula (II) R and R = H or alkali(ne earth) metal; R and R = 1-10C alkyl; A = nitrogen or phosphorus; Y = an anion; and R - R = 1-20C alkyl, 6-15C aryl or 7-20C aralkyl An Independent claim is also included for the novel compound 3,4-ethylenedioxythiophene-2,5-dicarboxylic acid monohydrate. |
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Also claimed is the novel compound 3,4-ethylenedioxythiophene-2,5-dicarboxylic acid monohydrate. Reaction of 3,4-dihydroxythiophene-2,5-dicarboxylic esters of formula (I) with alkylating agents in a polar diluent is effected in presence of a quaternary onium salt of formula (II) R and R = H or alkali(ne earth) metal; R and R = 1-10C alkyl; A = nitrogen or phosphorus; Y = an anion; and R - R = 1-20C alkyl, 6-15C aryl or 7-20C aralkyl An Independent claim is also included for the novel compound 3,4-ethylenedioxythiophene-2,5-dicarboxylic acid monohydrate.</description><edition>7</edition><language>eng ; fre ; ger</language><subject>APPARATUS THEREFOR ; CHEMISTRY ; GENERAL METHODS OF ORGANIC CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2005</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20050119&DB=EPODOC&CC=EP&NR=1298133B1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25564,76547</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20050119&DB=EPODOC&CC=EP&NR=1298133B1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>KLAUSENER, ALEXANDER DR</creatorcontrib><creatorcontrib>WINKLER, ADOLF DR</creatorcontrib><creatorcontrib>SCHENKEL, RALFO DR</creatorcontrib><creatorcontrib>BREMEN, JOSEF DR</creatorcontrib><creatorcontrib>RAUCHSCHWALBE, GUENTER DR</creatorcontrib><title>Procedure for the alkylation of 3,4-dihydroxythiophene-2,5-dicarboxylic esters</title><description>Reaction of 3,4-dihydroxythiophene-2,5-dicarboxylic esters with alkylating agents in a polar diluent is effected in presence of a quaternary onium salt. Also claimed is the novel compound 3,4-ethylenedioxythiophene-2,5-dicarboxylic acid monohydrate. Reaction of 3,4-dihydroxythiophene-2,5-dicarboxylic esters of formula (I) with alkylating agents in a polar diluent is effected in presence of a quaternary onium salt of formula (II) R and R = H or alkali(ne earth) metal; R and R = 1-10C alkyl; A = nitrogen or phosphorus; Y = an anion; and R - R = 1-20C alkyl, 6-15C aryl or 7-20C aralkyl An Independent claim is also included for the novel compound 3,4-ethylenedioxythiophene-2,5-dicarboxylic acid monohydrate.</description><subject>APPARATUS THEREFOR</subject><subject>CHEMISTRY</subject><subject>GENERAL METHODS OF ORGANIC CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2005</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZPALKMpPTk0pLUpVSMsvUijJSFVIzMmuzEksyczPU8hPUzDWMdFNycyoTCnKr6gsycjML8hIzUvVNdIxBQonJxYlAYVzMpMVUotLUouKeRhY0xJzilN5oTQ3g4Kba4izh25qQX58anFBYjJQc0m8a4ChkaWFobGxk6ExEUoAcaY1uw</recordid><startdate>20050119</startdate><enddate>20050119</enddate><creator>KLAUSENER, ALEXANDER DR</creator><creator>WINKLER, ADOLF DR</creator><creator>SCHENKEL, RALFO DR</creator><creator>BREMEN, JOSEF DR</creator><creator>RAUCHSCHWALBE, GUENTER DR</creator><scope>EVB</scope></search><sort><creationdate>20050119</creationdate><title>Procedure for the alkylation of 3,4-dihydroxythiophene-2,5-dicarboxylic esters</title><author>KLAUSENER, ALEXANDER DR ; WINKLER, ADOLF DR ; SCHENKEL, RALFO DR ; BREMEN, JOSEF DR ; RAUCHSCHWALBE, GUENTER DR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_EP1298133B13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre ; ger</language><creationdate>2005</creationdate><topic>APPARATUS THEREFOR</topic><topic>CHEMISTRY</topic><topic>GENERAL METHODS OF ORGANIC CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>KLAUSENER, ALEXANDER DR</creatorcontrib><creatorcontrib>WINKLER, ADOLF DR</creatorcontrib><creatorcontrib>SCHENKEL, RALFO DR</creatorcontrib><creatorcontrib>BREMEN, JOSEF DR</creatorcontrib><creatorcontrib>RAUCHSCHWALBE, GUENTER DR</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>KLAUSENER, ALEXANDER DR</au><au>WINKLER, ADOLF DR</au><au>SCHENKEL, RALFO DR</au><au>BREMEN, JOSEF DR</au><au>RAUCHSCHWALBE, GUENTER DR</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Procedure for the alkylation of 3,4-dihydroxythiophene-2,5-dicarboxylic esters</title><date>2005-01-19</date><risdate>2005</risdate><abstract>Reaction of 3,4-dihydroxythiophene-2,5-dicarboxylic esters with alkylating agents in a polar diluent is effected in presence of a quaternary onium salt. Also claimed is the novel compound 3,4-ethylenedioxythiophene-2,5-dicarboxylic acid monohydrate. Reaction of 3,4-dihydroxythiophene-2,5-dicarboxylic esters of formula (I) with alkylating agents in a polar diluent is effected in presence of a quaternary onium salt of formula (II) R and R = H or alkali(ne earth) metal; R and R = 1-10C alkyl; A = nitrogen or phosphorus; Y = an anion; and R - R = 1-20C alkyl, 6-15C aryl or 7-20C aralkyl An Independent claim is also included for the novel compound 3,4-ethylenedioxythiophene-2,5-dicarboxylic acid monohydrate.</abstract><edition>7</edition><oa>free_for_read</oa></addata></record> |
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subjects | APPARATUS THEREFOR CHEMISTRY GENERAL METHODS OF ORGANIC CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Procedure for the alkylation of 3,4-dihydroxythiophene-2,5-dicarboxylic esters |
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