IP Library Granted Patent US 8,530,709
Granted Patent B2
US 8,530,709 · App. 13/110,992 · Granted Sep 10, 2013

Process for the production of fluorinated alkenes

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Quick Facts
Patent No.
US 8,530,709
App. No.
13/110,992
Granted
Sep 10, 2013
Kind
B2
Abstract

The present invention provides a method for the preparation of suitable chlorofluorocarbon and hydrochlorofluorocarbon materials or chlorofluorocarbon and hydrochlorofluorocarbon alkene and alkyne intermediates which serve as useful feedstock for fluorination and reduction to cis-1,1,1,4,4,4-hexafluoro-2-butene. Also presented is a continuous process for the production of cis-1,1,1,4,4,4-hexafluoro-2-butene from the alkene and alkyne intermediates.

Claims (24)

1. A process for the manufacture of 1,1,1,4,4,4-hexafluoro-2-butene comprising the steps of:

(a) contacting a haloalkane compound with hexafluoropropene at a temperature effective to facilitate an addition reaction to form an intermediate hydrofluorochlorobutane;

(b) contacting HF with the intermediate hydrofluorochlorobutane formed in step (a) under conditions effective to facilitate the fluorination of the butane compound and produce an effluent stream comprising a compound selected from the group consisting of a hydrofluorobutane, a hydrofluorobutene, and mixtures thereof;

(c) contacting the reaction product of step (b) with a metal catalyst and hydrogen under conditions effective to dehydrohalogenate the reaction product of step (b) to form a compound selected from the group consisting of a hydrofluorobutene, a fluorobutyne, and mixtures thereof;

(d) recycling the reaction products of step (c) through the hydrogenation process to convert the hydrofluorobutene into hexafluorobutyne; and

(e) selectively reducing the hexafluorobutyne to produce the cis-1,1,1,4,4,4-hexafluoro-2-butene.

2. The process of claim 1 , wherein steps (a) and (b) are carried out in a continuous fashion.

3. The process of claim 1 , wherein the haloalkane compound has the formula:

CX n Y m Z o

wherein X, Y and Z are each independently selected from the group consisting of H, Cl and F and wherein the sum total of n+m+o=4.

4. The process of claim 3 , wherein the haloalkane compound is selected from the group consisting of CH 3 Cl, CH 2 Cl 2 , CHCl 3 , CCl 4 , CH 3 F, CH 2 F2, and CHF 2 Cl.

5. The process of claim 1 , wherein the intermediate hydrofluorochlorobutane is selected from the group consisting of CH 2 ClCF 2 CHFCF 3 , CHCl 2 CF 2 CHFCF 3 , CCl 3 CF 2 CHFCF 3 , CH 2 FCF 2 CHFCF 3 , CHF 2 CF 2 CHFCF 3 , and CF 2 ClCF 2 CHFCF 3 .

6. A process for the manufacture of fluorinated butenes comprising the steps of:

(a) an addition reaction between hexafluoropropene and a haloalkane compound having the formula:

CX n Y m Z o

wherein X, Y and Z are each independently selected from the group consisting of H, Cl and F and wherein the sum total of n+m+o=4 to produce an intermediate hydrofluorochlorobutane compound; and

(b) subjecting the intermediate hydrofluorochlorobutane compound to a reaction selected from the group consisting of chlorination, fluorination, dehydrohalogenation and one or more combinations of these reactions, to form one or more fluorinated butene compound.

7. The process of claim 6 , wherein the step (b) reaction comprises the chlorination of the intermediate hydrofluorochlorobutane compound.

8. The process of claim 6 , wherein the step (b) reaction comprises the fluorination of the intermediate hydrofluorochlorobutane compound.

9. The process of claim 6 , wherein the step (b) reaction comprises the dehydrohalogenation of the intermediate hydrofluorochlorobutane compound.

10. The process of claim 6 , further comprising step (c), the isolation of the fluorinated butene compound.

11. The process of claim 10 , wherein the isolation of the fluorinated butene compound is by distillation.

12. The process of claim 10 , wherein any unreacted starting materials are recycled.

13. The process of claim 6 , wherein the fluorinated butene compound is cis-1,1,1,4,4,4-hexafluorobutene (HFO-1336).

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 May 19, 2011
From: POSS, ANDREW JOSEPH; NALEWAJEK, DAVID; NAIR, HARIDASAN K.; VAN DER PUY, MICHAEL
To: HONEYWELL INTERNATIONAL INC.
Reel/Frame 026309/0377 →