Method for isomerizing organic compound, and method for producing isomer of organic compound

Patent metadata

Field	Value
Publication number	US-10703696-B2
Application number	US-201916389398-A
Country	US
Kind code	B2
Filing date	Apr 19, 2019
Priority date	Nov 1, 2016
Publication date	Jul 7, 2020
Grant date	Jul 7, 2020

Abstract

The method for isomerizing an organic compound comprises a step of selecting an alumina so that the acid amount calculated from the amount of ammonia desorbed at a desorption temperature of at least 300° C. by temperature-programmed desorption of ammonia is at least 0.10 mmol/g and at most 0.25 mmol/g; a step of fluorinating the selected alumina by a fluorinating agent to produce a partially fluorinated alumina; and a step of isomerizing, by using the obtained partially fluorinated alumina, an organic compound having at least two carbon atoms wherein to at least one of the adjacent carbon atoms, at least one fluorine atom is bonded and to the other, at least one chlorine atom or hydrogen atom is bonded.

First claim

What is claimed is:

1. A method for isomerizing a chlorofluorocarbon and/or a hydrofluorocarbon having at least two carbon atoms, comprising:
selecting an alumina in which an acid amount calculated from an amount of ammonia desorbed at a desorption temperature of at least 300° C. is at least 0.10 mmol/g and at most 0.25 mmol/g,
applying a fluorinating agent to the selected alumina to fluorinate the selected alumina and obtain a partially fluorinated alumina, and
contacting the chlorofluorocarbon and/or the hydrofluorocarbon having at least two carbon atoms with the obtained partially fluorinated alumina to interchange a position of a fluorine atom and a position of a chlorine atom or a hydrogen atom in the chlorofluorocarbon and/or the hydrofluorocarbon to isomerize the chlorofluorocarbon and/or a hydrofluorocarbon, wherein in the chlorofluorocarbon and/or a hydrofluorocarbon, to at least one of adjacent carbon atoms, at least one fluorine atom is bonded and to the other of the adjacent carbon atoms, at least one of chlorine atom and hydrogen atom is bonded.

2. The method according to claim 1 , wherein the fluorinating agent is an organic compound having at least two carbon atoms.

3. The method according to claim 1 , wherein the fluorinating agent is a fluorine compound other than an organic compound having at least two carbon atoms, or hydrogen fluoride.

4. The method according to claim 1 , wherein in a gas phase, the alumina is fluorinated by the fluorinating agent to obtain the partially fluorinated alumina.

5. The method according to claim 1 , wherein the acid amount is at least 0.15 mmol/g and at most 0.25 mmol/g.

6. The method according to claim 1 , wherein the organic compound is a hydrofluorochloropropane.

7. The method according to claim 6 , wherein the hydrofluorochloropropane comprises 1,3-dichloro-1,1,2,2,3-pentafluoropropane, and by the isomerization, 3,3-dichloro-1,1,1,2,2-pentafluoropropane is obtained.

8. The method according to claim 1 , wherein the acid amount is at least 0.102 mmol/g and at most 0.200 mmol/g.

9. The method for according to claim 1 , wherein the alumina has a γ-Al 2 O 3 structure.

10. The method according to claim 9 , wherein in a gas phase, the alumina is fluorinated by the fluorinating agent to obtain the partially fluorinated alumina.

11. The method according to claim 10 , wherein the acid amount is at least 0.15 mmol/g and at most 0.25 mmol/g.

12. The method according to claim 10 , wherein the organic compound is a hydrofluorochloropropane.

13. The method according to claim 12 , wherein the hydrofluorochloropropane comprises 1,3-dichloro-1,1,2,2,3-pentafluoropropane, and by the isomerization, 3,3-dichloro-1,1,1,2,2-pentafluoropropane is obtained.

14. The method according to claim 13 , wherein the acid amount is at least 0.102 mmol/g and at most 0.200 mmol/g.

15. The method according to claim 10 , wherein the acid amount is at least 0.102 mmol/g and at most 0.200 mmol/g.

16. The method according to claim 9 , wherein the acid amount is at least 0.15 mmol/g and at most 0.25 mmol/g.

17. The method according to claim 9 , wherein the organic compound is a hydrofluorochloropropane.

18. The method according to claim 17 , wherein the hydrofluorochloropropane comprises 1,3-dichloro-1,1,2,2,3-pentafluoropropane, and by the isomerization, 3,3-dichloro-1, 1,1,2,2-pentafluoropropane is obtained.

19. The method according to claim 9 , wherein the acid amount is at least 0.102 mmol/g and at most 0.200 mmol/g.

Assignees

• Agc Inc

Inventors

• Yamada Taku
• Suzuki Yusuke
• Kasagawa Mitsugu

Classifications

• C07B61/00

  Other general methods · CPC title

• C07C17/358 Primary

  by isomerisation · CPC title

• C07B2200/09

  Geometrical isomers · CPC title

• B01J27/125

  with scandium, yttrium, aluminium, gallium, indium or thallium · CPC title

• C07C19/10

  and chlorine · CPC title