US2019047924A1PendingUtilityA1

Method for producing fluorinated organic compounds

Assignee: HONEYWELL INT INCPriority: Jan 3, 2006Filed: Mar 5, 2018Published: Feb 14, 2019
Est. expiryJan 3, 2026(expired)· nominal 20-yr term from priority
C07C 17/087C07C 17/013C07C 19/10
72
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Claims

Abstract

Provided is a process for making 2-chloro-1,1,1,2-tetrafluoropropane. The process has the step of hydrofluorinating 2-chloro-3,3,3-trifluoropropene in the presence of a catalyst selected from the group consisting of SbCl3, SbCl5, SbF5, TiCl4, SnCl4, Cr2O3, and fluorinated Cr2O3.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A process for making 2-chloro-1,1,1,2-tetrafluoropropane, comprising hydrofluorinating 2-chloro-3,3,3-trifluoropropene in the presence of a catalyst selected from the group consisting of SbCl 3 , SbCl 5 , SbF 5 , TiCl 4 , SnCl 4 , Cr 2 O 3 , and fluorinated Cr 2 O 3 . 
     
     
         2 . The process of  claim 1 , wherein the catalyst is in bulk form. 
     
     
         3 . The process of  claim 1 , wherein the catalyst is supported. 
     
     
         4 . The process of  claim 3 , wherein the support is selected from the group consisting of carbon, alumina, fluorinated alumina, or aluminum fluoride. 
     
     
         5 . The process of  claim 1  where the catalyst is activated using anhydrous hydrogen fluoride. 
     
     
         6 . The process of  claim 1  where the catalyst is activated using anhydrous chlorine. 
     
     
         7 . The process of  claim 1 , wherein the hydrofluorination is vapor-phase fluorination. 
     
     
         8 . The process of  claim 7 , wherein the catalyst for vapor-phase fluorination reaction is SbCl 5  supported on activated carbon. 
     
     
         9 . The process of  claim 7 , wherein the catalyst for vapor-phase fluorination reaction is Cr 2 O 3  bulk or supported. 
     
     
         10 . The process of  claim 7 , wherein the catalyst for vapor-phase fluorination reaction is fluorinated Cr 2 O 3  bulk or supported. 
     
     
         11 . The process of  claim 7 , wherein the vapor-phase fluorination reaction is carried out at a temperature of about 50° C. to about 120° C. and at a pressure of about 30 psia to about 175 psia. 
     
     
         12 . The process of  claim 7 , wherein the mole ratio of hydrogen fluoride to 2-chloro-3,3,3-trifluoropropene is from about 2:1 to about 15:1. 
     
     
         13 . The process of  claim 1 , wherein the hydrofluorination is liquid-phase fluorination. 
     
     
         14 . The process of  claim 13 , wherein the catalyst for liquid-phase fluorination reaction is SbCl 5 . 
     
     
         15 . The process of  claim 13 , wherein the liquid-phase fluorination reaction is carried out at a temperature of about 50° C. to about 120° C. and at a pressure of about 50 psia to about 175 psia. 
     
     
         16 . The process of  claim 13 , wherein the mole ratio of hydrogen fluoride to 2-chloro-3,3,3-trifluoropropene is from about 2:1 to about 15:1.

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