C07C19/12

COMPOSITION COMPRISING 1-CHLORO-2,2-DIFLUOROETHANE AND 1,1-DICHLOROETHYLENE
20210309594 · 2021-10-07 · ·

Azeotropic and quasi-azeotropic compositions comprising 1-chloro-2,2-difluoroethane and 1,1-dichloroethylene. Also, a method for producing compositions comprising 1-chloro-2,2-difluoroethane and 1,1-dichloroethylene. The composition may include from 1 mol % to 99 mol % of 1-chloro-2,2-difluoroethane and from 99 mol % to 1 mol % of 1,1-dichloroethylene on the basis of the total composition thereof expressed in moles and the boiling point of the composition may be between 30° C. and 116° C.

COMPOSITIONS COMPRISING 2,3-DICHLORO-1,1,1-TRIFLUOROPROPANE, 2-CHLORO-1,1,1-TRIFLUOROPROPENE, 2-CHLORO-1,1,1,2-TETRAFLUOROPROPANE OR 2,3,3,3-TETRAFLUOROPROPENE

Disclosed are compositions comprising HCFC-243db, HCFO-1233xf, HCFC-244db and/or HFO-1234yf and at least one to additional compound. For the composition comprising 1234yf, the additional compound is selected from the group consisting of HFO-1234ze, HFO-1243zf, HCFC-243db, HCFC-244db, HFC-245cb, HFC-245fa, HCFO-1233xf, HCFO-1233zd, HCFC-253fb, HCFC-234ab, HCFC-243fa, ethylene, HFC-23, CFC-13, HFC-143a, HFC-152a, HFC-236fa, HCO-1130, HCO-1130a, HFO-1336, HCFC-133a, HCFC-254fb, CHF═CHCl, HFO-1141, HCFO-1242zf, HCFO-1223xd, HCFC-233ab, HCFC-226ba, and HFC-227ca. Compositions comprising HCFC-243db, HCFO-1233xf, and/or HCFC-244db are useful in processes to make HFO-1234yf. Compositions comprising HFO-1234yf are useful, among other uses, as heat transfer compositions for use in refrigeration, air-conditioning and heat pump systems.

COMPOSITIONS COMPRISING 2,3-DICHLORO-1,1,1-TRIFLUOROPROPANE, 2-CHLORO-1,1,1-TRIFLUOROPROPENE, 2-CHLORO-1,1,1,2-TETRAFLUOROPROPANE OR 2,3,3,3-TETRAFLUOROPROPENE

Disclosed are compositions comprising HCFC-243db, HCFO-1233xf, HCFC-244db and/or HFO-1234yf and at least one to additional compound. For the composition comprising 1234yf, the additional compound is selected from the group consisting of HFO-1234ze, HFO-1243zf, HCFC-243db, HCFC-244db, HFC-245cb, HFC-245fa, HCFO-1233xf, HCFO-1233zd, HCFC-253fb, HCFC-234ab, HCFC-243fa, ethylene, HFC-23, CFC-13, HFC-143a, HFC-152a, HFC-236fa, HCO-1130, HCO-1130a, HFO-1336, HCFC-133a, HCFC-254fb, CHF═CHCl, HFO-1141, HCFO-1242zf, HCFO-1223xd, HCFC-233ab, HCFC-226ba, and HFC-227ca. Compositions comprising HCFC-243db, HCFO-1233xf, and/or HCFC-244db are useful in processes to make HFO-1234yf. Compositions comprising HFO-1234yf are useful, among other uses, as heat transfer compositions for use in refrigeration, air-conditioning and heat pump systems.

Process for the manufacture of 1,1,1-trifluoro-2-chloroethaneand/or trifluoroethylamine
11046637 · 2021-06-29 ·

The invention relates to a new process for the manufacture of fluoroaryl compounds and derivatives thereof, in particular of fluorobenzenes and derivatives thereof, and especially wherein said manufacture relates to an environmentally friendly production of the said compounds. Thus, the present invention overcomes the disadvantages of the prior art processes, and in a surprisingly simple and beneficial manner, and as compared to the prior art processes, in particular, the invention provides a more efficient and energy saving processes, and also provides a more environmentally friendly process, for the manufacture of nuclear fluorinated aromatics, and preferably of nuclear fluorinated fluorobenzenes. Accordingly, in one aspect of the invention, an industrially beneficial process for preparing fluorobenzenes from halobenzene precursors using HF to form hydrogen halide is provided by the present invention. A beneficial and surprisingly simple use of chlorobenzene as an industrially interesting starting material in the manufacture of fluorobenzene is provided.

Process for the manufacture of 1,1,1-trifluoro-2-chloroethaneand/or trifluoroethylamine
11046637 · 2021-06-29 ·

The invention relates to a new process for the manufacture of fluoroaryl compounds and derivatives thereof, in particular of fluorobenzenes and derivatives thereof, and especially wherein said manufacture relates to an environmentally friendly production of the said compounds. Thus, the present invention overcomes the disadvantages of the prior art processes, and in a surprisingly simple and beneficial manner, and as compared to the prior art processes, in particular, the invention provides a more efficient and energy saving processes, and also provides a more environmentally friendly process, for the manufacture of nuclear fluorinated aromatics, and preferably of nuclear fluorinated fluorobenzenes. Accordingly, in one aspect of the invention, an industrially beneficial process for preparing fluorobenzenes from halobenzene precursors using HF to form hydrogen halide is provided by the present invention. A beneficial and surprisingly simple use of chlorobenzene as an industrially interesting starting material in the manufacture of fluorobenzene is provided.

Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene

Disclosed are compositions comprising HCFC-243db, HCFO-1233xf, HCFC-244db and/or HFO-1234yf and at least one additional compound. For the composition comprising 1234yf, the additional compound is selected from the group consisting of HFO-1234ze, HFO-1243zf, HCFC-243db, HCFC-244db, HFC-245cb, HFC-245fa, HCFO-1233xf, HCFO-1233zd, HCFC-253fb, HCFC-234ab, HCFC-243fa, ethylene, HFC-23, CFC-13, HFC-143a, HFC-152a, HFC-236fa, HCO-1130, HCO-1130a, HFO-1336, HCFC-133a, HCFC-254fb, CHF═CHCl, HFO-1141, HCFO-1242zf, HCFO-1223xd, HCFC-233ab, HCFC-226ba, and HFC-227ca. Compositions comprising HCFC-243db, HCFO-1233xf, and/or HCFC-244db are useful in processes to make HFO-1234yf. Compositions comprising HFO-1234yf are useful, among other uses, as heat transfer compositions for use in refrigeration, air-conditioning and heat pump systems.

Compositions comprising 2,3-dichloro-1,1,1-trifluoropropane, 2-chloro-1,1,1-trifluoropropene, 2-chloro-1,1,1,2-tetrafluoropropane or 2,3,3,3-tetrafluoropropene

Disclosed are compositions comprising HCFC-243db, HCFO-1233xf, HCFC-244db and/or HFO-1234yf and at least one additional compound. For the composition comprising 1234yf, the additional compound is selected from the group consisting of HFO-1234ze, HFO-1243zf, HCFC-243db, HCFC-244db, HFC-245cb, HFC-245fa, HCFO-1233xf, HCFO-1233zd, HCFC-253fb, HCFC-234ab, HCFC-243fa, ethylene, HFC-23, CFC-13, HFC-143a, HFC-152a, HFC-236fa, HCO-1130, HCO-1130a, HFO-1336, HCFC-133a, HCFC-254fb, CHF═CHCl, HFO-1141, HCFO-1242zf, HCFO-1223xd, HCFC-233ab, HCFC-226ba, and HFC-227ca. Compositions comprising HCFC-243db, HCFO-1233xf, and/or HCFC-244db are useful in processes to make HFO-1234yf. Compositions comprising HFO-1234yf are useful, among other uses, as heat transfer compositions for use in refrigeration, air-conditioning and heat pump systems.

BIOSOURCED VINYLIDENE DIFLUORIDE MONOMER AND POLYMERS CONTAINING IT
20210147325 · 2021-05-20 ·

The invention relates to biosourced vinylidene difluoride. The invention also relates to methods for preparation of biosourced vinylidene difluoride from various renewable raw materials. The invention also relates to homopolymers of vinylidene difluoride obtained from polymerization of said monomer, and also copolymers obtained by copolymerization of said monomer with one or several compatible comonomers. Finally, the invention relates to the use of said homopolymers or copolymers in applications, such as chemical engineering or electronics, in particular mass-market electronic devices.

BIOSOURCED VINYLIDENE DIFLUORIDE MONOMER AND POLYMERS CONTAINING IT
20210147325 · 2021-05-20 ·

The invention relates to biosourced vinylidene difluoride. The invention also relates to methods for preparation of biosourced vinylidene difluoride from various renewable raw materials. The invention also relates to homopolymers of vinylidene difluoride obtained from polymerization of said monomer, and also copolymers obtained by copolymerization of said monomer with one or several compatible comonomers. Finally, the invention relates to the use of said homopolymers or copolymers in applications, such as chemical engineering or electronics, in particular mass-market electronic devices.

METHOD FOR PREPARING 1,2-DIFLUOROETHYLENE AND/OR 1,1,2-TRIFLUOROETHANE
20210163381 · 2021-06-03 · ·

This invention relates to a method for preparing 1,2-difluoroethylene and/or 1,1,2-trifluoroethane, comprising a step of performing at least one fluorination reaction by bringing at least one halide selected from the group consisting of haloethanes represented by general formula (1) CHX.sup.1X.sup.2CH.sub.2X.sup.3 (wherein X.sup.1, X.sup.2, and X.sup.3 are the same or different, and represent Cl, Br, or F) and haloethylenes represented by general formula (2) CHX.sup.4═CHX.sup.5 (wherein X.sup.4 and X.sup.5 are the same or different, and represent Cl, Br or F, with the proviso that the case in which X.sup.4 and X.sup.5 are both F is excluded).