IP Library Granted Patent US 9,676,688
Granted Patent B2
US 9,676,688 · App. 15/370,352 · Granted Jun 13, 2017

Method for producing 1,1-dichloro-3,3,3-trifluoropropane

Inventors: Yu Takeuchi (Chiyoda-ku, JP); Shoji Furuta (Chiyoda-ku, JP)
Assignee: Asahi Glass Company, Limited
C07C17/278C07C17/272C07C19/08C07C19/10
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Quick Facts
Patent No.
US 9,676,688
App. No.
15/370,352
Granted
Jun 13, 2017
Kind
B2
Abstract

To provide a method for obtaining 1,1-dichloro-3,3,3-trifluoropropane by reacting 1,1-difluoroethylene with dichlorofluoromethane, which suppresses the production of chloroform as a by-product and achieves a product having a high R-243fa concentration. This method is characterized by obtaining 1,1-dichloro-3,3,3-trifluoropropane by reacting 1,1-difluoroethylene with dichlorofluoromethane in the presence of trifluoromethane.

Claims (14)

1. A method for producing 1,1-dichloro-3,3,3-trifluoropropane, which comprises reacting 1,1-difluoroethylene with dichlorofluoromethane in the presence of trifluoromethane, to obtain 1,1-dichloro-3,3,3-trifluoropropane.

2. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 1 , wherein the amount of trifluoromethane used relative to the amount of dichlorofluoromethane used, is from 10 ppm to 10% by molar ratio.

3. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 1 , wherein the amount of trifluoromethane used relative to the amount of 1,1-difluoroethylene used, is from 10 ppm to 10% by molar ratio.

4. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 1 , wherein trifluoromethane is continuously or intermittently supplied to the reaction system.

5. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 1 , wherein trifluoromethane is present in the reactor before initiation of the reaction.

6. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 1 , wherein the ratio of 1,1-difluoroethylene relative to dichlorofluoromethane is from 0.5 to 1.5 by molar ratio.

7. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 1 , wherein the reaction temperature is from −80 to 200° C.

8. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 1 , wherein the reaction is carried out in the presence of a catalyst.

9. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 8 , wherein the catalyst is a Lewis acid catalyst.

10. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 1 , wherein 1,1-dichloro-3,3,3-trifluoropropane and 1,3-dichloro-1,3,3-trifluoropropane are produced by the reaction.

11. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 10 , wherein the proportion of 1,1-dichloro-3,3,3-trifluoropropane relative to the total amount (100 mol %) of 1,1-dichloro-3,3,3-trifluoropropane and 1,3-dichloro-1,3,3-trifluoropropane, is from 50 to 95 mol %.

12. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 1 , wherein the reaction is carried out in a liquid phase.

13. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 12 , wherein the solvent in the reaction system is 1,1-dichloro-3,3,3-trifluoropropane.

14. The method for producing 1,1-dichloro-3,3,3-trifluoropropane according to claim 13 , wherein 1,1-dichloro-3,3,3-trifluoropropane is present in the reactor before initiation of the reaction, so as to form the liquid phase together with 1,1-dichloro-3,3,3-trifluoropropane produced by the reaction.

Assignments (2)
CHANGE OF NAME Recorded Aug 7, 2018
From: ASAHI GLASS COMPANY, LIMITED
To: AGC INC.
Reel/Frame 046730/0786 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 6, 2016
From: TAKEUCHI, YU; FURUTA, SHOJI
To: ASAHI GLASS COMPANY, LIMITED
Reel/Frame 040536/0083 →
Priority Claims (1)
JP 2014-117747 · Jun 6, 2014 · national
Continuity (2)
Continuation PCTJP2015064933 · May 25, 2015
Related Publication 20170081264A1 · Mar 23, 2017