Method of fluorination in the gaseous phase

Patent metadata

Field	Value
Publication number	US-9783471-B2
Application number	US-201415023475-A
Country	US
Kind code	B2
Filing date	Sep 17, 2014
Priority date	Sep 24, 2013
Publication date	Oct 10, 2017
Grant date	Oct 10, 2017

Abstract

The present invention concerns a method of producing at least one compound of formula (II): CF 3 —CX(Z)n-CHX(Z)n in which X represents, independently, a hydrogen, fluorine or chlorine atom, Z represents, independently, a hydrogen or fluorine atom, and n=0 or 1, from at least one compound of formula (I): CX(Y)2-CX(Y)m-CHmXY in which X and Y represent, independently, a hydrogen, fluorine or chlorine atom and m=0 or 1. The method comprises at least one step during which at least one compound of formula (I) reacts with HF in the gaseous phase in the presence of a fluorination catalyst in order to give at least one compound of formula (II), characterized in that the catalyst is made from chromium oxyfluoride containing at least nickel as the co-metal and at least one rare earth metal.

First claim

The invention claimed is:

1. A process for manufacturing at least one compound of formula (II): CF 3 —CX(Z) n —CHX(Z) n in which X independently represents a hydrogen, fluorine or chlorine atom, Z independently represents a hydrogen or fluorine atom and n=0 or 1, comprising at least one step during which at least one compound of formula (I): CX(Y) 2 —CX(Y) m —CH m XY in which X and Y independently represent a hydrogen, fluorine or chlorine atom and m=0 or 1, reacts with HF in the gaseous phase in the presence of a fluorination catalyst, characterized in that the catalyst is based on chromium oxyfluoride containing at least nickel as co-metal and at least one rare-earth metal.

2. The process as claimed in claim 1 , characterized in that the compounds of formula (II) are chosen from 2,3,3,3-tetrafluoropropene, 1,3,3,3-tetrafluoropropene, 1-chloro-3,3,3-trifluoro-1-propene, and 2-chloro-3,3,3-trifluoro-1-propene.

3. The process as claimed in claim 1 , characterized in that the compounds of formula (I) are chosen from 1,1,2,3-tetrachloropropene, 2,3,3,3-tetrachloropropene, 1,1,3,3-tetrachloropropene, 1,3,3,3-tetrachloropropene, 1,1,1,2,3-pentachloropropane, 1,1,1,3,3-pentachloropropane, 1,1,2,2,3-pentachloropropane, 1,2-dichloro-3,3,3-trifluoropropane, 2-chloro-2,3,3,3-tetrafluoropropane, 1,1,1,2,2-pentafluoropropane, 1-chloro-1,3,3,3-tetrafluoropropane and 1,1,1,3,3-pentafluoropropane.

4. The process as claimed in claim 1 , characterized in that 2,3,3,3-tetrafluoropropene is manufactured from halopropanes of formulae CX 3 CHClCH 2 X and CX 3 CFXCH 3 , halopropenes of formulae CX 3 CCl═CH 2 , CClX 2 CCl═CH 2 and CX 2 ═CClCH 2 X, with X independently representing a fluorine or chlorine atom.

5. The process as claimed in claim 1 , characterized in that 2,3,3,3-tetrafluoropropene is manufactured from 1,1,1,2,3-pentachloropropane, 1,1,2,3-tetrachloropropene, 1,1,1,2,2-pentafluoropropane and/or 2-chloro-3,3,3-trifluoro-1-propene.

6. The process as claimed in claim 2 , characterized in that 1,3,3,3-tetrafluoropropene is manufactured from 1,1,1,3,3-pentachloropropane, 1,1,3,3-tetrachloropropene, 1,1,1,3,3-pentafluoropropane and/or 1-chloro-3,3,3-trifluoro-1-propene.

7. The process as claimed in claim 2 , characterized in that 1-chloro-3,3,3-trifluoro-1-propene is manufactured from 1,1,1,3,3-pentachloropropane and/or 1,1,3,3-tetrachloropropene.

8. The process as claimed in claim 1 , characterized in that the rare-earth metal(s) are chosen from cerium, lanthanum and praseodymium.

9. The process as claimed in claim 1 , characterized in that the atomic ratio of rare-earth metal(s)/chromium in the catalyst is between 0.001-0.1, preferably between 0.001-0.02.

10. The process as claimed in claim 1 , characterized in that the nickel co-metal/chromium atomic ratio in the catalyst is between 0.5 and 5 and preferably between 0.7 and 2.

11. The process as claimed in claim 1 , characterized in that the catalyst is supported.

12. The process as claimed in claim 11 , characterized in that the support is chosen from charcoal, magnesium derivatives, alumina or aluminum derivatives.

13. The process as claimed in claim 1 , characterized in that the mole ratio of HF relative to the compounds of formula (I) to be reacted is between 5 and 40, preferably between 10 and 25.

14. The process as claimed in claim 1 , characterized in that the fluorination temperature is between 180 and 420° C., preferably between 280 and 420° C.

15. The process as claimed in claim 1 , characterized in that the catalyst is subjected to at least one activation step using a stream comprising HF.

Assignees

• Arkema France

Inventors

• Wendlinger Laurent

Classifications

• C07C17/206 Primary

  the other compound being HX · CPC title

• C07C17/20 Primary

  of halogen atoms by other halogen atoms · CPC title

• C07C17/25

  by splitting-off hydrogen halides from halogenated hydrocarbons · CPC title

• C07C21/18

  containing fluorine · CPC title