Método para preparar compuestos orgánicos fluorados
Un método para producir compuestos orgánicos fluorados, que comprende convertir un compuesto de Fórmula (IAA) CH2>=CClCF3 (IAA) en un compuesto de Fórmula (IB) CH3CClFCF3 (IB) y deshidrohalogenar dicho compuesto de Fórmula (IB) para formar un compuesto de Fórmula (II) CF3CF>=CH2 (II). Disclose...
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creator | Dubey, Rajesh Van der Puy, Michael Merkel, Daniel Phillips, Steven Bortz, Cheryl Light, Barbara Ma, Jing Mukhopahyay, Sudip Tung, Hsueh |
description | Un método para producir compuestos orgánicos fluorados, que comprende convertir un compuesto de Fórmula (IAA) CH2>=CClCF3 (IAA) en un compuesto de Fórmula (IB) CH3CClFCF3 (IB) y deshidrohalogenar dicho compuesto de Fórmula (IB) para formar un compuesto de Fórmula (II) CF3CF>=CH2 (II).
Disclosed are processes for the production of fluorinated olefins, preferably adapted to commercialization of CF3CF=CH2 (1234yf). Three steps may be used in preferred embodiments in which a feedstock such as CCl2=CClCH2Cl (which may be purchased or synthesized from 1,2,3-trichloropropane) is fluorinated (preferably with HF in gas-phase in the presence of a catalyst) to synthesize a compound such as CFaCCI=CH2, preferably in a 80-96% selectivity. The CF3CCl=CH2 is preferably converted to CF3CFClCH3 (244-isomer) using a SbCl5 as the catalyst which is then transformed selectively to 1234yf, preferably in a gas-phase catalytic reaction using activated carbon as the catalyst. For the first step, a mixture of Cr2O3 and FeCl3/C is preferably used as the catalyst to achieve high selectivity to CF3CCl=CH2 (96%). In the second step, SbCls/C is preferably used as the selective catalyst for transforming 1233xf to 244-isomer, CF3CFClCH3. The intermediates are preferably isolated and purified by distillation and used in the next step without further purification, preferably to a purity level of greater than about 95%. |
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Disclosed are processes for the production of fluorinated olefins, preferably adapted to commercialization of CF3CF=CH2 (1234yf). Three steps may be used in preferred embodiments in which a feedstock such as CCl2=CClCH2Cl (which may be purchased or synthesized from 1,2,3-trichloropropane) is fluorinated (preferably with HF in gas-phase in the presence of a catalyst) to synthesize a compound such as CFaCCI=CH2, preferably in a 80-96% selectivity. The CF3CCl=CH2 is preferably converted to CF3CFClCH3 (244-isomer) using a SbCl5 as the catalyst which is then transformed selectively to 1234yf, preferably in a gas-phase catalytic reaction using activated carbon as the catalyst. For the first step, a mixture of Cr2O3 and FeCl3/C is preferably used as the catalyst to achieve high selectivity to CF3CCl=CH2 (96%). In the second step, SbCls/C is preferably used as the selective catalyst for transforming 1233xf to 244-isomer, CF3CFClCH3. The intermediates are preferably isolated and purified by distillation and used in the next step without further purification, preferably to a purity level of greater than about 95%.</description><language>spa</language><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS ; ADHESIVES ; CHEMISTRY ; DYES ; MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE ; METALLURGY ; MISCELLANEOUS APPLICATIONS OF MATERIALS ; MISCELLANEOUS COMPOSITIONS ; NATURAL RESINS ; ORGANIC CHEMISTRY ; PAINTS ; POLISHES</subject><creationdate>2018</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=20180404&DB=EPODOC&CC=ES&NR=2661827T3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,780,885,25563,76418</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=20180404&DB=EPODOC&CC=ES&NR=2661827T3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>Dubey, Rajesh</creatorcontrib><creatorcontrib>Van der Puy, Michael</creatorcontrib><creatorcontrib>Merkel, Daniel</creatorcontrib><creatorcontrib>Phillips, Steven</creatorcontrib><creatorcontrib>Bortz, Cheryl</creatorcontrib><creatorcontrib>Light, Barbara</creatorcontrib><creatorcontrib>Ma, Jing</creatorcontrib><creatorcontrib>Mukhopahyay, Sudip</creatorcontrib><creatorcontrib>Tung, Hsueh</creatorcontrib><title>Método para preparar compuestos orgánicos fluorados</title><description>Un método para producir compuestos orgánicos fluorados, que comprende convertir un compuesto de Fórmula (IAA) CH2>=CClCF3 (IAA) en un compuesto de Fórmula (IB) CH3CClFCF3 (IB) y deshidrohalogenar dicho compuesto de Fórmula (IB) para formar un compuesto de Fórmula (II) CF3CF>=CH2 (II).
Disclosed are processes for the production of fluorinated olefins, preferably adapted to commercialization of CF3CF=CH2 (1234yf). Three steps may be used in preferred embodiments in which a feedstock such as CCl2=CClCH2Cl (which may be purchased or synthesized from 1,2,3-trichloropropane) is fluorinated (preferably with HF in gas-phase in the presence of a catalyst) to synthesize a compound such as CFaCCI=CH2, preferably in a 80-96% selectivity. The CF3CCl=CH2 is preferably converted to CF3CFClCH3 (244-isomer) using a SbCl5 as the catalyst which is then transformed selectively to 1234yf, preferably in a gas-phase catalytic reaction using activated carbon as the catalyst. For the first step, a mixture of Cr2O3 and FeCl3/C is preferably used as the catalyst to achieve high selectivity to CF3CCl=CH2 (96%). In the second step, SbCls/C is preferably used as the selective catalyst for transforming 1233xf to 244-isomer, CF3CFClCH3. The intermediates are preferably isolated and purified by distillation and used in the next step without further purification, preferably to a purity level of greater than about 95%.</description><subject>ACYCLIC OR CARBOCYCLIC COMPOUNDS</subject><subject>ADHESIVES</subject><subject>CHEMISTRY</subject><subject>DYES</subject><subject>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</subject><subject>METALLURGY</subject><subject>MISCELLANEOUS APPLICATIONS OF MATERIALS</subject><subject>MISCELLANEOUS COMPOSITIONS</subject><subject>NATURAL RESINS</subject><subject>ORGANIC CHEMISTRY</subject><subject>PAINTS</subject><subject>POLISHES</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>2018</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZDD1PbyyJD8lX6EgsShRoaAoFUQXKSTn5xaUphaX5Bcr5BelH16Yl5kMZKbllOYXJabkF_MwsKYl5hSn8kJpbgZFN9cQZw_d1IL8-NTigsTk1LzUknjXYCMzM0MLI_OQEGNjYtQAAFFOL5c</recordid><startdate>20180404</startdate><enddate>20180404</enddate><creator>Dubey, Rajesh</creator><creator>Van der Puy, Michael</creator><creator>Merkel, Daniel</creator><creator>Phillips, Steven</creator><creator>Bortz, Cheryl</creator><creator>Light, Barbara</creator><creator>Ma, Jing</creator><creator>Mukhopahyay, Sudip</creator><creator>Tung, Hsueh</creator><scope>EVB</scope></search><sort><creationdate>20180404</creationdate><title>Método para preparar compuestos orgánicos fluorados</title><author>Dubey, Rajesh ; Van der Puy, Michael ; Merkel, Daniel ; Phillips, Steven ; Bortz, Cheryl ; Light, Barbara ; Ma, Jing ; Mukhopahyay, Sudip ; Tung, Hsueh</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_ES2661827TT33</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>spa</language><creationdate>2018</creationdate><topic>ACYCLIC OR CARBOCYCLIC COMPOUNDS</topic><topic>ADHESIVES</topic><topic>CHEMISTRY</topic><topic>DYES</topic><topic>MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE</topic><topic>METALLURGY</topic><topic>MISCELLANEOUS APPLICATIONS OF MATERIALS</topic><topic>MISCELLANEOUS COMPOSITIONS</topic><topic>NATURAL RESINS</topic><topic>ORGANIC CHEMISTRY</topic><topic>PAINTS</topic><topic>POLISHES</topic><toplevel>online_resources</toplevel><creatorcontrib>Dubey, Rajesh</creatorcontrib><creatorcontrib>Van der Puy, Michael</creatorcontrib><creatorcontrib>Merkel, Daniel</creatorcontrib><creatorcontrib>Phillips, Steven</creatorcontrib><creatorcontrib>Bortz, Cheryl</creatorcontrib><creatorcontrib>Light, Barbara</creatorcontrib><creatorcontrib>Ma, Jing</creatorcontrib><creatorcontrib>Mukhopahyay, Sudip</creatorcontrib><creatorcontrib>Tung, Hsueh</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Dubey, Rajesh</au><au>Van der Puy, Michael</au><au>Merkel, Daniel</au><au>Phillips, Steven</au><au>Bortz, Cheryl</au><au>Light, Barbara</au><au>Ma, Jing</au><au>Mukhopahyay, Sudip</au><au>Tung, Hsueh</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Método para preparar compuestos orgánicos fluorados</title><date>2018-04-04</date><risdate>2018</risdate><abstract>Un método para producir compuestos orgánicos fluorados, que comprende convertir un compuesto de Fórmula (IAA) CH2>=CClCF3 (IAA) en un compuesto de Fórmula (IB) CH3CClFCF3 (IB) y deshidrohalogenar dicho compuesto de Fórmula (IB) para formar un compuesto de Fórmula (II) CF3CF>=CH2 (II).
Disclosed are processes for the production of fluorinated olefins, preferably adapted to commercialization of CF3CF=CH2 (1234yf). Three steps may be used in preferred embodiments in which a feedstock such as CCl2=CClCH2Cl (which may be purchased or synthesized from 1,2,3-trichloropropane) is fluorinated (preferably with HF in gas-phase in the presence of a catalyst) to synthesize a compound such as CFaCCI=CH2, preferably in a 80-96% selectivity. The CF3CCl=CH2 is preferably converted to CF3CFClCH3 (244-isomer) using a SbCl5 as the catalyst which is then transformed selectively to 1234yf, preferably in a gas-phase catalytic reaction using activated carbon as the catalyst. For the first step, a mixture of Cr2O3 and FeCl3/C is preferably used as the catalyst to achieve high selectivity to CF3CCl=CH2 (96%). In the second step, SbCls/C is preferably used as the selective catalyst for transforming 1233xf to 244-isomer, CF3CFClCH3. The intermediates are preferably isolated and purified by distillation and used in the next step without further purification, preferably to a purity level of greater than about 95%.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | ACYCLIC OR CARBOCYCLIC COMPOUNDS ADHESIVES CHEMISTRY DYES MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FORELSEWHERE METALLURGY MISCELLANEOUS APPLICATIONS OF MATERIALS MISCELLANEOUS COMPOSITIONS NATURAL RESINS ORGANIC CHEMISTRY PAINTS POLISHES |
title | Método para preparar compuestos orgánicos fluorados |
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