IP Library Granted Patent US 8,395,001
Granted Patent B2
US 8,395,001 · App. 13/157,370 · Granted Mar 12, 2013

Processes for producing 2-chloro-1,1,1,2-tetrafluoropropane and 2,3,3,3-tetrafluoropropene

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Quick Facts
Patent No.
US 8,395,001
App. No.
13/157,370
Granted
Mar 12, 2013
Kind
B2
Abstract

To provide processes for efficiently and economically producing 2-chloro-1,1,1,2-tetrafluoropropane (R244bb) and 2,3,3,3-tetrafluoropropene (R1234yf) in an industrially practical manner. A process for producing 2-chloro-1,1,1,2-tetrafluoropropane, which comprises a chlorination step of reacting 1,2-dichloro-2-fluoropropane and chlorine in the presence of a solvent under irradiation with light to obtain 1,1,1,2-tetrachloro-2-fluoropropane, and a fluorination step of reacting the 1,1,1,2-tetrachloro-2-fluoropropane obtained in the chlorination step and hydrogen fluoride in the presence of a catalyst to obtain 2-chloro-1,1,1,2-tetrafluoropropane, and a process for producing 2,3,3,3-tetrafluoropropene, which comprises dehydrochlorinating it in the presence of a catalyst.

Claims (28)

1. A process for producing 2-chloro-1,1,1,2-tetrafluoropropane, comprising:

a chlorination step of reacting 1,2-dichloro-2-fluoropropane and chlorine in the presence of a solvent under irradiation with light to obtain 1,1,1,2-tetrachloro-2-fluoropropane, and

a fluorination step of reacting the 1,1,1,2-tetrachloro-2-fluoropropane obtained in the chlorination step and hydrogen fluoride in the presence of a catalyst to obtain 2-chloro-1,1,1,2-tetrafluoropropane,

wherein the solvent comprises at least one member selected from the group consisting of carbon tetrachloride, 1,1,2-trichloro-1,2,2-trifluoroethane, a C 5-8 linear perfluoroalkyl compound represented by the formula CF 3 (CF 2 ) n CF 3 , wherein n is an integer of from 3 to 6, and a perhalogenated compound, and

wherein the catalyst comprises at least one halide of a metal selected from the group consisting of antimony, niobium, tantalum, tin, titanium, iron and thallium.

2. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 1 , wherein the solvent in the chlorination step is carbon tetrachloride.

3. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 1 , wherein the light for the irradiation with light in the chlorination step is ultraviolet light containing light with a wavelength of from 200 to 400 nm.

4. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 1 , wherein the reaction temperature in the chlorination step is from −20 to 60° C.

5. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 1 , wherein the catalyst in the fluorination step is a catalyst for fluorination is at least one halide of a metal selected from antimony, niobium, tantalum, tin, titanium, iron and thallium.

6. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 1 , wherein the reaction temperature in the fluorination step is from 50 to 200° C.

7. A process for producing 2,3,3,3-tetrafluoropropene, which comprises subjecting the 2-chloro-1,1,1,2-tetrafluoropropane obtained in claim 1 to a dehydrochlorination in the presence of a catalyst comprising at least one member selected from the group consisting of activated carbon and a nickel catalyst.

8. The process for producing 2,3,3,3-tetrafluoropropene according to claim 7 , wherein the catalyst comprises the the nickel catalyst.

9. The process for producing 2,3,3,3-tetrafluoropropene according to claim 7 , wherein the reaction temperature for the dehydrochlorination reaction is from 200 to 700° C.

10. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 1 , wherein the catalyst is antimony pentachloride.

11. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 1 , wherein the solvent comprises carbon tetrachloride and the catalyst is antimony pentachloride.

12. A process for producing 2-chloro-1,1,1,2-tetrafluoropropane, comprising:

reacting 1,2-dichloro-2-fluoropropane with chlorine in the presence of a solvent under irradiation with light to produce 1,1,1,2-tetrachloro-2-fluoropropane, and

reacting the 1,1,1,2-tetrachloro-2-fluoropropane with hydrogen fluoride in the presence of a catalyst to obtain 2-chloro-1,1,1,2-tetrafluoropropane,

wherein the solvent comprises at least one member selected from the group consisting of carbon tetrachloride, 1,1,2-trichloro-1,2,2-trifluoroethane, a C 5-8 linear perfluoroalkyl compound represented by the formula CF 3 (CF 2 ) n CF 3 , wherein n is an integer of from 3 to 6, and a perhalogenated compound, and

wherein the catalyst comprises at least one halide of a metal selected from the group consisting of antimony, niobium, tantalum, tin, titanium, iron and thallium.

13. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 12 , wherein the light for the irradiation with light in the reacting with chlorine is ultraviolet light containing light with a wavelength of from 200 to 400 nm.

14. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 12 , wherein the reaction temperature in the reacting with chlorine is from -20 to 60° C.

15. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 12 , wherein the reaction temperature in the reacting with hydrogen fluoride is from 50 to 200° C.

16. A process for producing 2,3,3,3-tetrafluoropropene, which comprises dehydrochlorinating the 2-chloro-1,1,1,2-tetrafluoropropane obtained in claim 12 in the presence of a catalyst comprising at least one member selected from the group consisting of activated carbon and a nickel catalyst.

17. The process for producing 2,3,3,3-tetrafluoropropene according to claim 16 , wherein the reaction temperature in the dehydrochlorinating is from 200 to 700° C.

18. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according claim 12 , wherein the solvent comprises carbon tetrachloride.

19. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according claim 12 , wherein the catalyst is antimony pentachloride.

20. The process for producing 2-chloro-1,1,1,2-tetrafluoropropane according to claim 12 , wherein the solvent comprises carbon tetrachloride and the catalyst is antimony pentachloride.

Assignments (3)
CHANGE OF NAME Recorded Aug 7, 2018
From: ASAHI GLASS COMPANY, LIMITED
To: AGC INC.
Reel/Frame 046730/0786 →
CORPORATE ADDRESS CHANGE Recorded Nov 9, 2011
From: ASAHI GLASS COMPANY, LIMITED
To: ASAHI GLASS COMPANY, LIMITED
Reel/Frame 027197/0541 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 10, 2011
From: KAWAGUCHI, SATOSHI; OKAZOE, TAKASHI; OKAMOTO, HIDEKAZU
To: ASAHI GLASS COMPANY, LIMITED
Reel/Frame 026422/0889 →