IP Library Granted Patent US 10,807,925
Granted Patent B2
US 10,807,925 · App. 14/721,575 · Granted Oct 20, 2020

Preparation of fluorinated olefins via catalytic dehydrohalogenation of halogenated hydrocarbons

Inventors: Haiyou Wang (Amherst, NY); Hsueh Sung Tung (Getzville, NY)
Assignee: Honeywell International Inc.
C07C17/25B01J27/10B01J27/12B01J27/138B01J35/0006C07B35/06
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Quick Facts
Patent No.
US 10,807,925
App. No.
14/721,575
Granted
Oct 20, 2020
Kind
B2
Abstract

A process for making a fluorinated olefin having the step of dehydrochlorinating a hydrochlorofluorocarbon having at least one hydrogen atom and at least one chlorine atom on adjacent carbon atoms, preferably carried out in the presence of a catalyst selected from the group consisting of (i) one or more metal halides, (ii) one or more halogenated metal oxides, (iii) one or more zero-valent metals/metal alloys, (iv) a combination of two or more of the foregoing.

Claims (21)

1. A process for making a three carbon fluorinated olefin, comprising: dehydrochlorinating a three carbon hydrochlorofluorocarbon having at least one hydrogen and at least one chlorine on adjacent carbons in the presence of a catalyst selected from one or more zero-valent metal alloys, wherein the zero-valent metal alloy comprises Pd, Pt, Rh, Fe, Co, Ni, Mo, Cr, Mn, and combinations of these; and

wherein the hydrochlorofluorocarbon and resulting fluorinated olefin is selected from the group consisting of 1,1,1,2-tetrafluoro-2-chloropropane and 2,3,3,3-tetrafluoropropene, 1,1,1,2-tetrafluoro-3-chloropropane and 2,3,3,3-tetrafluoropropene, 1,1,1,3-tetrafluoro-3-chloropropane and 1,3,3,3-tetrafluoropropene, 1,1,1,3-tetrafluoro-2-chloropropane and 1,3,3,3-tetrafluoropropene, 1,1,1,2,3-pentafluoro-2-chloropropane and 1,2,3,3,3-pentafluoropropene, 1,1,1,2,3-pentafluoro-3-chloropropane and 1,2,3,3,3-pentafluoropropene, 1,1,1,3,3-pentafluoro-3-chloropropane and 1,1,3,3,3-pentafluoropropene.

2. The process of claim 1 , wherein the hydrochlorofluorocarbon is 1,1,1,2-tetrafluoro-2-chloropropane and the fluorinated olefin is 2,3,3,3-tetrafluoropropene.

3. The process of claim 1 , wherein the one or more zero-valent metal alloys is a Ni alloy.

4. The process of claim 1 , wherein said zero valent metal alloy is selected from SS 316, Monel 400, lnconel 825, lnconel 600 and lnconel 625.

5. The process of claim 1 , wherein dehydrochlorination is carried out at a temperature of from about 300 to about 600° C.

6. The process of claim 1 , wherein dehydrochlorination is carried out at a temperature of from about 400 to about 500° C.

7. The process of claim 6 , wherein the catalyst comprises Ni.

8. The process of claim 1 , wherein the catalyst comprises Ni.

9. The process of claim 1 , wherein the catalyst comprises lnconel 600.

10. The process of claim 9 , wherein the catalyst comprises lnconel 600 chips.

11. The process of claim 1 , wherein said zero valent metal alloy is selected from lnconel 600 and lnconel 625.

12. The process of claim 1 , wherein said zero valent metal alloy is lnconel 600.

13. The process of claim 1 , wherein said zero valent metal alloy is lnconel 625.

14. A process for making a fluorinated olefin, comprising: dehydrochlorinating a hydrochlorofluorocarbon having at least one hydrogen and at least one chlorine on adjacent carbons in the presence of catalyst comprising a zero valent metal alloy selected from Inconel 625 and Inconel 600.

15. The process of claim 14 , wherein dehydrochlorination is carried out at a temperature of from about 300 to about 600° C.

16. The process of claim 14 , wherein dehydrochlorination is carried out at a temperature of from about 400 to about 500° C.

17. The process of claim 14 , wherein said zero valent metal alloy is lnconel 600.

18. The process of claim 14 , wherein said zero valent metal alloy is lnconel 625.

19. The process of claim 14 , wherein the hydrochlorofluorocarbon and resulting fluorinated olefin is selected from the group consisting of 1,1,1,2-tetrafluoro-2-chloropropane and 2,3,3,3-tetrafluoropropene, 1,1,1,2-tetrafluoro-3-chloropropane and 2,3,3,3-tetrafluoropropene, 1,1,1,3-tetrafluoro-3-chloropropane and 1,3,3,3-tetrafluoropropene, 1,1,1,3-tetrafluoro-2-chloropropane and 1,3,3,3-tetrafluoropropene, 1,1,1,2,3-pentafluoro-2-chloropropane and 1,2,3,3,3-pentafluoropropene, 1,1,1,2,3-pentafluoro-3-chloropropane and 1,2,3,3,3-pentafluoropropene, 1,1,1,3,3-pentafluoro-3-chloropropane and 1,1,3,3,3-pentafluoropropene.

20. The process of claim 14 , wherein the hydrochlorofluorocarbon is 1,1,1,2-tetrafluoro-2-chloropropane and the fluorinated olefin is 2,3,3,3-tetrafluoropropene.

Assignments (2)
SECURITY INTEREST Recorded Jan 12, 2026
From: SOLSTICE ADVANCED MATERIALS US, INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 074569/0260 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 4, 2025
From: WANG, HAIYOU; TUNG, HSUEH SUNG
To: HONEYWELL INTERNATIONAL INC.
Reel/Frame 070399/0593 →