Process for preparing dialkyl and diaryl phosphonothioic halides
Dialkyl or diaryl phosphonothioic halides are prepared by contacting an alkyl or aryl halide, respectively, with phosphorus sesquisulfide, P4S3, under at least autogenous pressure at a temperature of from about 200 DEG to about 400 DEG C. The compounds obtained are useful as pesticides and as interm...
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creator | TOY ARTHUR D. F UHING EUGENE H |
description | Dialkyl or diaryl phosphonothioic halides are prepared by contacting an alkyl or aryl halide, respectively, with phosphorus sesquisulfide, P4S3, under at least autogenous pressure at a temperature of from about 200 DEG to about 400 DEG C. The compounds obtained are useful as pesticides and as intermediates in preparation of pesticides and other organo-phosphorus compounds. |
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F ; UHING; EUGENE H</creatorcontrib><description>Dialkyl or diaryl phosphonothioic halides are prepared by contacting an alkyl or aryl halide, respectively, with phosphorus sesquisulfide, P4S3, under at least autogenous pressure at a temperature of from about 200 DEG to about 400 DEG C. The compounds obtained are useful as pesticides and as intermediates in preparation of pesticides and other organo-phosphorus compounds.</description><language>eng</language><subject>ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1978</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=19780228&DB=EPODOC&CC=US&NR=4076746A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25544,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19780228&DB=EPODOC&CC=US&NR=4076746A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>TOY; ARTHUR D. F</creatorcontrib><creatorcontrib>UHING; EUGENE H</creatorcontrib><title>Process for preparing dialkyl and diaryl phosphonothioic halides</title><description>Dialkyl or diaryl phosphonothioic halides are prepared by contacting an alkyl or aryl halide, respectively, with phosphorus sesquisulfide, P4S3, under at least autogenous pressure at a temperature of from about 200 DEG to about 400 DEG C. 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F</creatorcontrib><creatorcontrib>UHING; EUGENE H</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>TOY; ARTHUR D. F</au><au>UHING; EUGENE H</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Process for preparing dialkyl and diaryl phosphonothioic halides</title><date>1978-02-28</date><risdate>1978</risdate><abstract>Dialkyl or diaryl phosphonothioic halides are prepared by contacting an alkyl or aryl halide, respectively, with phosphorus sesquisulfide, P4S3, under at least autogenous pressure at a temperature of from about 200 DEG to about 400 DEG C. The compounds obtained are useful as pesticides and as intermediates in preparation of pesticides and other organo-phosphorus compounds.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAININGELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN,SULFUR, SELENIUM OR TELLURIUM CHEMISTRY METALLURGY ORGANIC CHEMISTRY |
title | Process for preparing dialkyl and diaryl phosphonothioic halides |
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