IP Library Granted Patent US 7,799,959
Granted Patent B2
US 7,799,959 · App. 12/298,843 · Granted Sep 21, 2010

Process for producing 1,2,3,4-tetrachlorohexafluorobutane

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Quick Facts
Patent No.
US 7,799,959
App. No.
12/298,843
Granted
Sep 21, 2010
Kind
B2
Abstract

Disclosed is a process for producing 1,2,3,4-tetrachlorohexafluorobutane safely in a high yield in the industrial viewpoint and at low cost in the economical viewpoint. Specifically disclosed is a process for producing 1,2,3,4-tetrachlorohexafluorobutane which process comprises: (1) a step of chlorinating 1,3-butadiene, thereby preparing a mixture containing 1,2,3,4-tetrachlorobutane, and (2) a step of allowing the 1,2,3,4-tetrachlorobutane prepared in the step (1) to react with a fluorine gas in the presence of a diluting gas in a gas phase, thereby preparing a mixture containing 1,2,3,4-tetrachlorohexafluorobutane.

Claims (25)

1. A process for producing 1,2,3,4-tetrachlorohexafluorobutane which process comprises:

(1) a step of chlorinating 1,3-butadiene, thereby preparing a mixture containing 1,2,3,4-tetrachlorobutane, and

(2) a step of allowing the 1,2,3,4-tetrachlorobutane prepared in the step (1) to react with a fluorine gas in the presence of a diluting gas in a gas phase, thereby preparing a mixture containing 1,2,3,4-tetrachlorohexafluorobutane.

2. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 1 wherein the step (2) comprises allowing the 1,2,3,4-tetrachlorobutane prepared in the step (1) to react with a fluorine gas in the absence of a catalyst, thereby preparing a mixture containing 1,2,3,4-tetrachlorohexafluorobutane.

3. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 1 wherein the step (1) comprises chlorinating 1,3-butadiene, thereby preparing a mixture containing 1,2,3,4-tetrachlorobutane and 3,4-dichlorobutene-1.

4. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 3 wherein the 1,2,3,4-tetrachlorobutane is a by-product.

5. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 1 which process further comprises:

(3) a step of separating 1,2,3,4-tetrachlorobutane from the mixture containing 1,2,3,4-tetrachlorobutane prepared in the step (1),

wherein the step (2) comprises allowing the 1,2,3,4-tetrachlorobutane prepared in the step (3) to react with a fluorine gas thereby preparing a mixture containing 1,2,3,4-tetrachlorohexafluorobutane.

6. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 1 which process further comprises:

(4) a step of separating 3,4-dichlorobutene-1 from the mixture containing 1,2,3,4-tetrachlorobutane prepared in the step (1) and

(5) a step of chlorinating the 3,4 dichlorobutene-1 prepared in the step (4), thereby preparing 1,2,3,4-tetrachlorobutane,

wherein the step (2) comprises allowing the 1,2,3,4-tetrachlorobutane prepared in the step (5) to react with a fluorine gas, thereby preparing a mixture containing 1,2,3,4-tetrachlorohexafluorobutane.

7. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 1 wherein the diluting gas is at least one gas selected from the group consisting of nitrogen, helium, argon, neon and hydrogen fluoride.

8. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 5 or 6 wherein the step (2) comprises allowing 1,2,3,4-tetrachlorobutane to react with a fluorine gas in a reactor having at least two feed openings by feeding a mixed gas (A) of 1,2,3,4-tetrachlorobutane prepared in the step (3) or (5) and the diluting gas from at least one feed opening and feeding a mixed gas (B) of a fluorine gas and the diluting gas from at least one of the other openings, thereby preparing a mixture containing 1,2,3,4-tetrachlorohexafluorobutane, and the concentration of 1,2,3,4-tetrachlorobutane is from 0.5 to 4% by mole based on the total amount of the mixed gases (A) and (B).

9. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 5 or 6 wherein the step (2) comprises allowing 1,2,3,4-tetrachlorobutane to react with a fluorine gas in a reactor having at least two feed openings by feeding a mixed gas (A) of 1,2,3,4-tetrachlorobutane prepared in the step (3) or (5) and the diluting gas from at least one feed opening and feeding a mixed gas (B) of a fluorine gas and the diluting gas from at least one of the other openings, thereby preparing a mixture containing 1,2,3,4-tetrachlorohexafluorobutane, and the concentration of a fluorine gas is from 0.5 to 10% by mole based on the total amount of the mixed gases (A) and (B).

10. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 5 or 6 wherein the step (2) comprises allowing the 1,2,3,4-tetrachlorobutane prepared in the step (3) or (5) to react with a fluorine gas at a pressure of from 0.05 to 1 MPa, thereby preparing a mixture containing 1,2,3,4-tetrachlorohexafluorobutane.

11. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 5 or 6 wherein the step (2) comprises allowing the 1,2,3,4-tetrachlorobutane prepared in the step (3) or (5) to react with a fluorine gas at a temperature of from 50 to 500° C., thereby preparing a mixture containing 1,2,3,4-tetrachlorohexafluorobutane.

12. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 8 which process further comprises:

(6) a step of liquid-liquid separating the mixture containing 1,2,3,4-tetrachlorohexafluorobutane prepared in the step (2) and allowing a resulting 1,2,3,4-tetrachlorohexafluorobutane-rich phase to contact with an alkali, thereby preparing crude 1,2,3,4-tetrachlorohexafluorobutane, and

(7) a step of dehydrating the crude 1,2,3,4-tetrachlorohexafluorobutane prepared in the step (6), thereby preparing crude 1,2,3,4-tetrachlorohexafluorobutane.

13. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 9 which process further comprises:

(6) a step of liquid-liquid separating the mixture containing 1,2,3,4-tetrachlorohexafluorobutane prepared in the step (2) and allowing a resulting 1,2,3,4-tetrachlorohexafluorobutane-rich phase to contact with an alkali, thereby preparing crude 1,2,3,4-tetrachlorohexafluorobutane, and

(7) a step of dehydrating the crude 1,2,3,4-tetrachlorohexafluorobutane prepared in the step (6), thereby preparing crude 1,2,3,4-tetrachlorohexafluorobutane.

14. The process for producing 1,2,3,4-tetrachlorohexafluorobutane according to claim 12 or 13 which further comprises (8) a step of feeding the crude 1,2,3,4-tetrachlorohexafluorobutane prepared in the step (7), to at least one distillation column, separating an intermediate in the reaction of step (2) and feeding at least a part of the intermediate to the reactor.

Assignments (3)
CHANGE OF ADDRESS Recorded Feb 14, 2024
From: RESONAC CORPORATION
To: RESONAC CORPORATION
Reel/Frame 066599/0037 →
CHANGE OF NAME Recorded Jun 23, 2023
From: SHOWA DENKO K.K.
To: RESONAC CORPORATION
Reel/Frame 064082/0513 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 30, 2009
From: OHNO, HIROMOTO; OHI, TOSHIO
To: SHOWA DENKO K.K.
Reel/Frame 022183/0498 →