IP Library Granted Patent US 9,440,896
Granted Patent B2
US 9,440,896 · App. 14/416,313 · Granted Sep 13, 2016

Dehydrochlorination of HCFC-336 isomers to 1,1,1,4,4,4-hexafluoro-2-butyne

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Quick Facts
Patent No.
US 9,440,896
App. No.
14/416,313
Granted
Sep 13, 2016
Kind
B2
Abstract

Disclosed is a process for producing hexafluoro-2-butyne comprising, reacting HCFC-336 with an aqueous solution of an alkali metal hydroxide in the presence of a quaternary alkylammonium salt which comprises at least one alkyl group of at least 8 carbons, and recovering the hexafluoro-2-butyne, wherein the conversion of dichloro-1,1,1,4,4,4-hexafluorobutane is at least 50% per hour. Also disclosed is a process for producing hexafluoro-2-butyne comprising, reacting HCFC-336 with an aqueous solution of an alkali metal hydroxide in the presence of a quaternary alkylammonium salt having alkyl groups of from four to ten carbon atoms, and mixtures thereof, and a non-ionic surfactant, and recovering the hexafluoro-2-butyne, and wherein the conversion of dichloro-1,1,1,4,4,4-hexafluorobutane to hexafluoro-2-butyne is at least 20% per hour.

Claims (13)

1. A process for producing hexafluoro-2-butyne comprising reacting Z-1,1,1,4,4,4-hexafluoro-2-chloro-2-butene with an aqueous solution of an alkali metal hydroxide comprising an alkali metal halide in the presence of a quaternary alkylammonium salt having alkyl groups of from four to twelve carbon atoms and mixtures thereof, to produce a mixture comprising hexafluoro-2-butyne, and recovering the hexafluoro-2-butyne, wherein the conversion of Z-1,1,1,4,4,4-hexafluoro-2-chloro-2-butene to hexafluoro-2-butyne is at least 50% per hour, wherein said reaction occurs at less than 100° C.

2. The process according to claim 1 , wherein said alkali metal halide is sodium chloride.

3. The process according to claim 1 wherein the aqueous solution is made from a base selected from the group consisting of lithium hydroxide, sodium hydroxide, potassium hydroxide, calcium hydroxide, magnesium oxide, calcium oxide, sodium carbonate, potassium carbonate, sodium phosphate, potassium phosphate, and mixtures thereof.

4. The process according to claim 1 , wherein the aqueous solution is made from sodium hydroxide or potassium hydroxide.

5. A process for producing hexafluoro-2-butyne comprising, reacting a fluorochloroolefin comprising E-1,1,1,4,4,4-hexafluoro-2-chloro-2-butene with an aqueous solution of an alkali metal hydroxide in the presence of a quaternary alkylammonium salt which comprises at least one alkyl group of at least 8 carbons, and recovering the hexafluoro-2-butyne, wherein the conversion of E-1,1,1,4,4,4-hexafluoro-2-chloro-2-butene to hexafluoro-2-butyne is at least 15% per hour, wherein said reaction occurs at less than 100° C.

6. The process according to claim 5 , wherein said alkali metal hydroxide further comprises an alkali metal halide.

7. The process according to claim 6 , wherein said alkali metal halide is sodium chloride.

8. The process according to claim 5 , wherein said quaternary alkylammonium salt has at least 3 alkyl groups of eight carbons or higher.

9. The process according to claim 5 , wherein said quaternary alkylammounium salt is methyltrioctylammonium chloride.

10. The process according to claim 9 , wherein the conversion of E-1,1,1,4,4,4-hexafluoro-2-chloro-2-butene to hexafluoro-2-butyne is at least 50% per hour.

11. The process according to claim 5 wherein the aqueous solution is made from a base selected from the group consisting of lithium hydroxide, sodium hydroxide, potassium hydroxide, calcium hydroxide, magnesium oxide, calcium oxide, sodium carbonate, potassium carbonate, sodium phosphate, potassium phosphate, and mixtures thereof.

12. The process according to claim 5 , wherein the aqueous solution is made from sodium hydroxide or potassium hydroxide.

13. The process according to claim 5 , wherein said fluorochloroolefin further comprises Z-1,1,1,4,4,4-hexafluoro-2-chloro-2-butene.

Assignments (1)
SECURITY INTEREST Recorded Apr 4, 2018
From: THE CHEMOURS COMPANY FC, LLC
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 045846/0011 →