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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Hauptverfasser: Dubey, Rajesh, Van der Puy, Michael, Merkel, Daniel, Phillips, Steven, Bortz, Cheryl, Light, Barbara, Ma, Jing, Mukhopahyay, Sudip, Tung, Hsueh
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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. 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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%.</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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