IP Library › Granted Patent US 8,779,222
Granted Patent B2
US 8,779,222 · App. 13/389,168 · Granted Jul 15, 2014

Method for producing 1,1,3-trichloro-1-propene

Inventors: Hiroshi Souda (Oita, JP); Koji Hagiya (Ibaraki, JP)
Assignee: Sumitomo Chemical Company, Limited
C07C17/25C07C17/358
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Quick Facts
Patent No.
US 8,779,222
App. No.
13/389,168
Granted
Jul 15, 2014
Kind
B2
Abstract

A production method of 1,1,3-trichloro-1-propene comprising the following steps A and B; Step A: 1,1,1,3-tetrachloropropane is dehydrochlorinated at a temperature between 30° C. and 50° C. in the presence of at least one base selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides, and a phase transfer catalyst, Step B: 3,3,3-trichloro-1-propene obtained in the step A is isomerized into 1,1,3-trichloro-1-propene in the presence of a metal catalyst.

Claims (25)

1. A method of producing 1,1,3-trichloro-1-propene comprising the following steps A and B;

Step A: 1,1,1,3-tetrachloropropane is dehydrochlorinated at a temperature between 30° C. and 50° C. in the presence of at least one base selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides, and a phase transfer catalyst,

Step B: 3,3,3-trichloro-1-propene obtained in the step A is isomerized into 1,1,3-trichloro-1-propene in the presence of a metal catalyst except of ferric chloride.

2. A method of producing 1,1,1,3-trichloro-1-propene comprising the following steps A and B;

Step A: 1,1,1,3-tetrachloropropane is dehydrochlorinated at a temperature between 30° C. and 50° C. in the presence of at least one base selected from the group consisting of alkali metal hydroxides and alkaline earth metal hydroxides, and a phase transfer catalyst, to obtain a mixture containing 1,1,3-trichloro-1-propene and 3,3,3-trichloro-1-propene;

Step B: the mixture containing 1,1,3-trichloro-1-propene and 3,3,3-trichloro-1-propene is allowed to contact with a metal catalyst except of ferric chloride to isomerize 3,3,3-trichloro-1-propene in said mixture into 1,1,1,3-trichloro-1-propene.

3. The method according to claim 1 , wherein the phase transfer catalyst is a quaternary ammonium salt or a quaternary phosphonium salt.

4. The method according to claim 1 , wherein a base aqueous solution is used as the base in the step A.

5. The method according to claim 1 , wherein a step C is carried out between the step A and the step B;

Step C: the reaction mixture obtained in the step A is washed with an acid, then washed with water.

6. The method according to claim 5 , wherein the acid is hydrochloric acid, sulfuric acid, phosphoric acid or nitric acid.

7. The method according to claim 1 , wherein the metal catalyst is a metal simple body or a metal compound containing at least one metal selected from the group consisting of group VII metals, group VIII metals, group IX metals, group X metals, group XI metals, group XII metals, group XIV metals and group XV metals in the periodic table.

8. The method according to claim 1 , wherein, the metal catalyst is a metal simple body or a metal compound containing at least one metal selected from the group consisting of iron, copper, zinc, silver, nickel, palladium, tin, bismuth and manganese.

9. The method according to claim 1 , wherein isomerization in the step B is carried out under a temperature between 50° C. and 120° C.

10. The method according to claim 1 , wherein the step A is carried out in the absence of an organic solvent.

11. The method according to claim 1 , wherein the step B is carried out in the absence of an organic solvent.

12. The method according to claim 2 , wherein the phase transfer catalyst is a quaternary ammonium salt or a quaternary phosphonium salt.

13. The method according to claim 2 , wherein a base aqueous solution is used as the base in the step A.

14. The method according to claim 2 , wherein a step C is carried out between the step A and the step B;

Step C: the reaction mixture obtained in the step A is washed with an acid, then washed with water.

15. The method according to claim 2 , wherein the metal catalyst is a metal simple body or a metal compound containing at least one metal selected from the group consisting of group VII metals, group VIII metals, group IX metals, group X metals, group XI metals, group XII metals, group XIV metals and group XV metals in the periodic table.

16. The method according to claim 2 , wherein the metal catalyst is a metal simple body or a metal compound containing at least one metal selected from the group consisting of iron, copper, zinc, silver, nickel, palladium, tin, bismuth and manganese.

17. The method according to claim 2 , wherein isomerization in the step B is carried out under a temperature between 50° C. and 120° C.

18. The method according to claim 2 , wherein the step A is carried out in the absence of an organic solvent.

19. The method according to claim 2 , wherein the step B is carried out in the absence of an organic solvent.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 6, 2012
From: SOUDA, HIROSHI; HAGIYA, KOJI
To: SUMITOMO CHEMICAL COMPANY, LIMITED
Reel/Frame 027658/0475 →
Priority Claims (1)
JP 2009-199763 · Aug 31, 2009 · national
Continuity (1)
Related Publication 20120142981A1 · Jun 7, 2012