FLUOROOLEFIN PRODUCTION METHOD

The present disclosure provides a method for producing fluoroolefin represented by formula (1): CX1X2=CX3X4, wherein X1, X2, X3, and X4 are the same or different, and represent a hydrogen atom or a fluorine atom, with high selectivity. Specifically, the present disclosure is a method for producing f...

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Hauptverfasser: NAKAUE, Tsubasa, USUI, Takashi, CHAKI, Takehiro
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creator NAKAUE, Tsubasa
USUI, Takashi
CHAKI, Takehiro
description The present disclosure provides a method for producing fluoroolefin represented by formula (1): CX1X2=CX3X4, wherein X1, X2, X3, and X4 are the same or different, and represent a hydrogen atom or a fluorine atom, with high selectivity. Specifically, the present disclosure is a method for producing fluoroolefin represented by formula (1), wherein the method includes the step of performing dehydrofluorination by bringing a fluorocarbon represented by formula (2) : CX1X2FCX3X4H, wherein X1, X2, X3, and X4 are as defined above, into contact with a base, and the dehydrofluorination step is performed in the liquid phase at a temperature of -70°C or higher to less than 120°C.
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Specifically, the present disclosure is a method for producing fluoroolefin represented by formula (1), wherein the method includes the step of performing dehydrofluorination by bringing a fluorocarbon represented by formula (2) : CX1X2FCX3X4H, wherein X1, X2, X3, and X4 are as defined above, into contact with a base, and the dehydrofluorination step is performed in the liquid phase at a temperature of -70°C or higher to less than 120°C.</description><language>eng ; fre ; ger</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; CHEMISTRY ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>2023</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&amp;date=20230927&amp;DB=EPODOC&amp;CC=EP&amp;NR=3778539B1$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25562,76317</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=20230927&amp;DB=EPODOC&amp;CC=EP&amp;NR=3778539B1$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>NAKAUE, Tsubasa</creatorcontrib><creatorcontrib>USUI, Takashi</creatorcontrib><creatorcontrib>CHAKI, Takehiro</creatorcontrib><title>FLUOROOLEFIN PRODUCTION METHOD</title><description>The present disclosure provides a method for producing fluoroolefin represented by formula (1): CX1X2=CX3X4, wherein X1, X2, X3, and X4 are the same or different, and represent a hydrogen atom or a fluorine atom, with high selectivity. Specifically, the present disclosure is a method for producing fluoroolefin represented by formula (1), wherein the method includes the step of performing dehydrofluorination by bringing a fluorocarbon represented by formula (2) : CX1X2FCX3X4H, wherein X1, X2, X3, and X4 are as defined above, into contact with a base, and the dehydrofluorination step is performed in the liquid phase at a temperature of -70°C or higher to less than 120°C.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>CHEMISTRY</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2023</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZJBz8wn1D_L393F18_RTCAjydwl1DvH091PwdQ3x8HfhYWBNS8wpTuWF0twMCm6uIc4euqkF-fGpxQWJyal5qSXxrgHG5uYWpsaWTobGRCgBAJaAIV8</recordid><startdate>20230927</startdate><enddate>20230927</enddate><creator>NAKAUE, Tsubasa</creator><creator>USUI, Takashi</creator><creator>CHAKI, Takehiro</creator><scope>EVB</scope></search><sort><creationdate>20230927</creationdate><title>FLUOROOLEFIN PRODUCTION METHOD</title><author>NAKAUE, Tsubasa ; USUI, Takashi ; CHAKI, Takehiro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_EP3778539B13</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng ; fre ; ger</language><creationdate>2023</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>CHEMISTRY</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>NAKAUE, Tsubasa</creatorcontrib><creatorcontrib>USUI, Takashi</creatorcontrib><creatorcontrib>CHAKI, Takehiro</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>NAKAUE, Tsubasa</au><au>USUI, Takashi</au><au>CHAKI, Takehiro</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>FLUOROOLEFIN PRODUCTION METHOD</title><date>2023-09-27</date><risdate>2023</risdate><abstract>The present disclosure provides a method for producing fluoroolefin represented by formula (1): CX1X2=CX3X4, wherein X1, X2, X3, and X4 are the same or different, and represent a hydrogen atom or a fluorine atom, with high selectivity. Specifically, the present disclosure is a method for producing fluoroolefin represented by formula (1), wherein the method includes the step of performing dehydrofluorination by bringing a fluorocarbon represented by formula (2) : CX1X2FCX3X4H, wherein X1, X2, X3, and X4 are as defined above, into contact with a base, and the dehydrofluorination step is performed in the liquid phase at a temperature of -70°C or higher to less than 120°C.</abstract><oa>free_for_read</oa></addata></record>
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subjects ACYCLIC OR CARBOCYCLIC COMPOUNDS
CHEMISTRY
METALLURGY
ORGANIC CHEMISTRY
title FLUOROOLEFIN PRODUCTION METHOD
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