PROCESSES FOR PREPARING PARTIALLY FLUORINATED EPOXIDES AND PERFLUORINATED EPOXIDES AND COMPOSITIONS RELATED THERETO
This application relates to the preparation of partially fluorinated epoxides and perfluorinated epoxides which may be useful in various applications including refrigerants, heat transfer media, high-temperature heat pumps, organic Rankine cycles, fire extinguishing/fire suppression, propellants, foam blowing, solvents, gaseous dielectrics, and/or cleaning fluids. Compositions comprising the fluorinated epoxide compounds are also provided.
1 . A process of preparing a compound of Formula (I):
comprising reacting a compound of Formula (II):
R 1 —C(R 2 )═C(R 3 )—R 4 (II)
with an aqueous hypohalite salt in the presence of a cationic phase transfer catalyst and an organic solvent, wherein:
R 1 and R 4 are each independently H, Cl, F, Br, I, a partially fluorinated C 1-4 alkoxy, or a perfluorinated C 1-4 alkoxy;
R 2 is selected from H, Cl, F, Br, I, a partially fluorinated C 1-10 alkyl, a perfluorinated C 1-10 alkyl, a partially fluorinated C 1-4 alkoxy, and a perfluorinated C 1-4 alkoxy;
wherein at least one of R 1 , R 2 , and R 4 is not H; and
R 3 is selected from partially fluorinated and perfluorinated C 1-10 alkyl;
or alternatively, R 2 and R 3 are each independently selected from partially fluorinated or perfluorinated C 1-5 alkylene, which together form a monocyclic ring.
2 . (canceled)
3 . (canceled)
4 . The process of claim 1 , wherein R 1 and R 4 are each independently H or F; and R 2 and R 3 are each independently selected from partially fluorinated or perfluorinated C 1-10 alkyl.
5 . The process of claim 1 , wherein the hypohalite salt is selected from NaOCl, KOCl, NaOBr, and Ca(OCl) 2 .
6 . (canceled)
7 . The process of claim 1 , wherein the cationic phase transfer catalyst is a quaternary ammonium salt or a quaternary phosphonium salt.
8 . (canceled)
9 . The process of claim 1 , the cationic phase transfer catalyst has formula (R a )(R b )(R c )(R d )N + X − or (R a )(R b )(R c )(R d )P + X − , wherein R a , R b , R c , and R 4 are each independently selected from C 1-18 alkyl, C 3-14 cycloalkyl, 4-14 membered heterocycloalkyl, C 6-14 aryl, 5-14 membered heteroaryl, C 3-14 cycloalkyl-C 1-3 alkylene, 4-14 membered heterocycloalkyl-C 1-3 alkylene, C 6-14 membered aryl-C 1-3 alkylene, and 5-14 membered heteroaryl-C 1-3 alkylene, each of which is optionally substituted by 1, 2, 3, or 4 groups independently selected from OH, C 1-6 alkoxy, C 1-6 alkyl, C 2-6 alkenyl, C 1-6 fluoroalkyl, di-(C 1-6 alkyl)amino, C 3-14 cycloalkyl, 4-14 membered heterocycloalkyl, C 6-14 membered aryl, and 5-14 membered heteroaryl; and X − is an anion.
10 . The process of claim 1 , wherein the cationic phase transfer catalyst has formula (R a )(R b )(R c )(R d )N + X − , wherein R a , R b , R c , and R 4 are eah independently selected from C 1-12 alkyl; and X is a halide ion or HSO 4 − .
11 . The process of claim 1 , wherein the cationic phase transfer catalyst has formula (R a )(R b )(R c )(R d )P + X − , wherein R a , R b , R c , and R d are each independently selected from C 1-12 alkyl or phenyl; and X is a halide ion or HSO 4 − .
12 . (canceled)
13 . The process of claim 1 , wherein the organic solvent is acetonitrile, tetrahydrofuran, diethyl ether, methyl-t-butyl ether, dimethyoxyethane, bis(2-methoxyethyl) ether, or benzene substituted with 1, 2, 3, or 4 independently selected C 1-4 alkyl groups.
14 . The process of claim 1 , wherein the organic solvent is acetonitrile or benzene substituted with 1, 2, 3, or 4 independently selected C 1-4 alkyl groups.
15 . The process of claim 1 , wherein the organic solvent is acetonitrile, toluene, o-xylene, m-xylene, p-xylene or a mixture thereof.
16 . (canceled)
17 . The process of claim 1 , wherein the reaction is conducted at a pH of from 10 to 14.
18 . The process of claim 1 , wherein the reaction is conducted at a temperature of from about 10° C. to about 30° C., from about 10° C. to about 20° C., from about 20° C. to about 30° C., or from about 25° C. to about 30° C.
19 . (canceled)
20 . (canceled)
21 . The process of claim 1 , wherein the compound of Formula (I) is selected from the group consisting of:
(Z)-2,3-difluoro-2-(trifluoromethyl)oxirane;
(E)-2,3-difluoro-2-(trifluoromethyl)oxirane;
cis-2-fluoro-3-(trifluoromethyl)oxirane;
trans-2-fluoro-3-(trifluoromethyl)oxirane;
trans-2,3-bis(trifluoromethyl)oxirane;
cis-2,3-bis(trifluoromethyl)oxirane;
trans-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane;
trans-2-(trifluoromethyl)-3-(perfluoropropan-2-yl)oxirane;
trans-2,3-bis(perfluoropropyl)oxirane;
trans-2-(perfluorobutyl)-3-(perfluoroethyl)oxirane;
trans-2,3-bis(perfluorobutyl)oxirane;
(Z)-2-(2,2,2-Trifluoroethoxy)-3-fluoro-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane;
(E)-2-(2,2,2-Trifluoroethoxy)-3-fluoro-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane;
cis-2,3-dichloro-2,3-bis(trifluoromethyl)oxirane;
trans-2,3-dichloro-2,3-bis(trifluoromethyl)oxirane;
trans-2-fluoro-3-(perfluoropropan-2-yl)oxirane;
cis-2-fluoro-3-(perfluoropropan-2-yl)oxirane;
cis-2,2,3,3,4,4-hexafluoro-6-oxa-bicyclo[3.1.0]hexane;
cis-2,2,3,3-tetrafluoro-5-oxabicyclo[2.1.0]pentane;
cis-2,3-difluoro-2-(perfluoroethyl)-3-(perfluoropropyl)oxirane;
trans-2,3-difluoro-2-(perfluoroethyl)-3-(perfluoropropyl)oxirane;
cis-2,3-difluoro-2-(trifluoromethyl)-3-(perfluoropentyl)oxirane; and
trans-2,3-difluoro-2-(trifluoromethyl)-3-(perfluoropentyl)oxirane.
22 . A composition comprising a compound of Formula I:
R 1 and R 4 are each independently H, Cl, F, Br, I, a partially fluorinated C 1-4 alkoxy, or a perfluorinated C 1-4 alkoxy;
R 2 is selected from H, Cl, F, Br, I, a partially fluorinated C 1-10 alkyl, a perfluorinated C 1-10 alkyl, a partially fluorinated C 1-4 alkoxy, and a perfluorinated C 1-4 alkoxy;
wherein at least one of R 1 , R 2 , and R 4 is not H; and
R 3 is selected from partially fluorinated and perfluorinated C 1-10 alkyl;
or alternatively, R 2 and R 3 are each independently selected from partially fluorinated or perfluorinated C 1-5 alkylene, which together form a monocyclic ring;
wherein the compound of Formula I has the (Z) or (E) configuration and the composition is substantially free of the opposite stereoisomers.
23 . A composition of claim 22 , wherein the composition comprises a compound selected from:
(Z)-2,3-difluoro-2-(trifluoromethyl)oxirane;
(E)-2,3-difluoro-2-(trifluoromethyl)oxirane;
cis-2-fluoro-3-(trifluoromethyl)oxirane;
trans-2-fluoro-3-(trifluoromethyl)oxirane;
trans-2,3-bis(trifluoromethyl)oxirane;
cis-2,3-bis(trifluoromethyl)oxirane;
trans-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane;
trans-2-(trifluoromethyl)-3-(perfluoropropan-2-yl)oxirane;
trans-2,3-bis(perfluoropropyl)oxirane;
trans-2-(perfluorobutyl)-3-(perfluoroethyl)oxirane;
trans-2,3-bis(perfluorobutyl)oxirane;
(Z)-2-(2,2,2-Trifluoroethoxy)-3-fluoro-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane;
(E)-2-(2,2,2-Trifluoroethoxy)-3-fluoro-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane;
cis-2,3-dichloro-2,3-bis(trifluoromethyl)oxirane;
trans-2,3-dichloro-2,3-bis(trifluoromethyl)oxirane;
trans-2-fluoro-3-(perfluoropropan-2-yl)oxirane;
cis-2-fluoro-3-(perfluoropropan-2-yl)oxirane;
cis-2,2,3,3,4,4-hexafluoro-6-oxa-bicyclo[3.1.0]hexane;
cis-2,2,3,3-tetrafluoro-5-oxabicyclo[2.1.0]pentane;
cis-2,3-difluoro-2-(perfluoroethyl)-3-(perfluoropropyl)oxirane;
trans-2,3-difluoro-2-(perfluoroethyl)-3-(perfluoropropyl)oxirane;
cis-2,3-difluoro-2-(trifluoromethyl)-3-(perfluoropentyl)oxirane; and
trans-2,3-difluoro-2-(trifluoromethyl)-3-(perfluoropentyl)oxirane.
24 . A compound selected from the group consisting of:
(Z)-2,3-difluoro-2-(trifluoromethyl)oxirane;
(E)-2,3-difluoro-2-(trifluoromethyl)oxirane;
cis-2-fluoro-3-(trifluoromethyl)oxirane;
trans-2-fluoro-3-(trifluoromethyl)oxirane;
trans-2,3-bis(trifluoromethyl)oxirane;
cis-2,3-bis(trifluoromethyl)oxirane;
trans-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane;
trans-2-(trifluoromethyl)-3-(perfluoropropan-2-yl)oxirane;
trans-2,3-bis(perfluoropropyl)oxirane;
trans-2-(perfluorobutyl)-3-(perfluoroethyl)oxirane;
trans-2,3-bis(perfluorobutyl)oxirane;
(Z)-2-(2,2,2-Trifluoroethoxy)-3-fluoro-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane;
(E)-2-(2,2,2-Trifluoroethoxy)-3-fluoro-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane;
cis-2,3-dichloro-2,3-bis(trifluoromethyl)oxirane;
trans-2,3-dichloro-2,3-bis(trifluoromethyl)oxirane;
trans-2-fluoro-3-(perfluoropropan-2-yl)oxirane;
cis-2-fluoro-3-(perfluoropropan-2-yl)oxirane;
cis-2,2,3,3,4,4-hexafluoro-6-oxa-bicyclo[3.1.0]hexane;
cis-2,2,3,3-tetrafluoro-5-oxabicyclo[2.1.0]pentane;
cis-2,3-difluoro-2-(perfluoroethyl)-3-(perfluoropropyl)oxirane;
trans-2,3-difluoro-2-(perfluoroethyl)-3-(perfluoropropyl)oxirane;
cis-2,3-difluoro-2-(trifluoromethyl)-3-(perfluoropentyl)oxirane; and
trans-2,3-difluoro-2-(trifluoromethyl)-3-(perfluoropentyl)oxirane.
25 . A composition comprising a compound of Formula (I):
and a compound of Formula (III):
R 5 —C(R 6 )═C(R 7 )—R 8 (III)
wherein:
the compounds of Formula (I) and Formula (III) have the same stereochemistry;
R 1 and R 5 are identical and are H, Cl, F, Br, I, a partially fluorinated C 1-4 alkoxy, or a perfluorinated C 1-4 alkoxy;
R 4 and R 8 are identical and each independently H, Cl, F, Br, I, a partially fluorinated C 1-4 alkoxy, or a perfluorinated C 1-4 alkoxy;
R 2 and R 6 are identical and are Cl, F, Br, I, partially fluorinated C 1-10 alkyl, or perfluorinated C 1-10 alkyl; and
R 3 and R 7 are identical and are partially fluorinated or perfluorinated C 1-10 alkyl; provided that either R 1 and R 5 are H or Cl; or R 4 and R 8 are H or Cl.
26 . A composition comprising a compound of Formula (I):
and a compound of Formula (III):
R 5 —C(R 6 )═C(R 7 )—R 8 (III)
wherein:
the compounds of Formula (I) and Formula (III) have the same stereochemistry;
R 1 and R 5 are identical and are H, Cl, F, Br, I, a partially fluorinated C 1-4 alkoxy, or a perfluorinated C 1-4 alkoxy;
R 4 and R 8 are identical and each independently H, Cl, F, Br, I, a partially fluorinated C 1-4 alkoxy, or a perfluorinated C 1-4 alkoxy;
R 2 and R 6 are identical and are partially fluorinated or perfluorinated C 1-5 alkylene; and
R 3 and R 7 are identical and are partially fluorinated or perfluorinated C 1-5 alkylene; wherein said R 2 and R 3 are taken together form a monocyclic ring and R 6 and R 7 are taken together form a monocyclic ring;
27 . The composition of claim 25 , wherein the molar ratio of the compound of Formula (I) to the compound of Formula (III) in the composition is from about 50:50 to about 99.:0.01
28 . (canceled)
29 . (canceled)
30 . The composition of claim 25 , wherein the composition comprises:
a compound of Formula (I) which is 2-fluoro-3-(trifluoromethyl)oxirane and a compound of Formula (III) which is 1,3,3,3-tetrafluoroprop-1-ene; or
a compound of Formula (I) which is 2,3-bis(trifluoromethyl)oxirane and a compound of Formula (III) which is 1,1,1,4,4,4-hexafluorobut-2-ene; or
a compound of Formula (I) which is 2-(trifluoromethyl)-3-(perfluoroethyl)oxirane and a compound of Formula (III) which is 1,1,1,4,4,5,5,5-octafluoropent-2-ene; or
a compound of Formula (I) which is 2-(trifluoromethyl)-3-(perfluoropropan-2-yl)oxirane and a compound of Formula (III) which is 1,1,1,5,5,5-hexafluoro-4,4-bis(trifluoromethyl)pent-2-ene; or
a compound of Formula (I) which is 2,3-bis(perfluoropropyl)oxirane and a compound of Formula (III) which is 1,1,1,2,2,3,3,6,6,7,7,8,8,8-tetradecafluorooct-4-ene; or
a compound of Formula (I) which is 2-(perfluorobutyl)-3-(perfluoroethyl)oxirane and a compound of Formula (III) which is 1,1,1,2,2,5,5,6,6,7,7,8,8,8-tetradecafluorooct-3-ene; or
a compound of Formula (I) which is 2,3-bis(perfluorobutyl)oxirane and a compound of Formula (III) which is 1,1,1,2,2,3,3,4,4,7,7,8,8,9,9,10,10,10-octadecafluorodec-5-ene; or
a compound of Formula (I) which is 2-(2,2,2-Trifluoroethoxy)-3-fluoro-2-(trifluoromethyl)-3-(perfluoroethyl)oxirane and a compound of Formula (III) which is 2-(2,2,2-trifluoroethoxy)-1,1,1,4,4,5,5,5-octafluoropent-2-ene; or
a compound of Formula (I) which is 2,3-dichloro-2,3-bis(trifluoromethyl)oxirane and a compound of Formula (III) which is 2,3-dichloro-1,1,1,4,4,4-hexafluorobut-2-ene; or
a compound of Formula (I) which is 2-fluoro-3-(perfluoropropan-2-yl)oxirane and a compound of Formula (III) which is 1,3,4,4,4-pentafluoro-3-(trifluoromethyl)but-1-ene; or
a compound of Formula (I) which is 2,3-difluoro-2-(perfluoroethyl)-3-(perfluoropropyl)oxirane and a compound of Formula (III) which is perfluoroheptene-3; or
a compound of Formula (I) which is 2,3-difluoro-2-(trifluoromethyl)-3-(perfluoropentyl)oxirane and a compound of Formula (III) which is perfluoroctene-2.
31 . The composition of claim 26 , wherein the composition comprises:
a compound of Formula (I) which is 2,2,3,3,4,4-hexafluoro-6-oxa-bicyclo[3.1.0]hexane and a compound of Formula (III) which is 3,3,4,4,5,5-hexafluorocyclopent-1-ene; or
a compound of Formula (I) which is 2,2,3,3-tetrafluoro-5-oxabicyclo[2.1.0]pentane and a compound of Formula (III) which is 3,3,4,4-tetrafluorocyclobut-1-ene.
32 . (canceled)
33 . (canceled)