Azeotropic or azeotrope-like compositions of 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd) and hydrogen fluoride (HF)
View Patent ↗Azeotropic or azeotrope-like mixtures of 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd) and hydrogen fluoride (HF). Such compositions are useful as a feed stock or intermediate in the production of 1,1,1,3,3-pentafluoropropane (HFC-245fa),1-chloro-3,3,3-trifluoropropene (HCFO-1233zd), and 1,3,3,3-tetrafluoropropene (HFO-1234ze).
1. An azeotropic or azeotrope-like composition consisting of 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd) and hydrogen fluoride (HF).
2. The composition of claim 1 , wherein the composition consists of from about 1 to about 99 wt. % hydrogen fluoride (HF) and from about 1 to about 99 wt. % 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd), based on the combined weight of the hydrogen fluoride (HF) and 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd).
3. The composition of claim 1 , wherein the composition consists of from about 2 to about 99 wt. % hydrogen fluoride (HF) and from about 1 to about 98 wt. % 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd), based on the combined weight of the hydrogen fluoride (HF) and 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd).
4. The composition of claim 1 , wherein the composition consists of from about 2 to about 80 wt. % hydrogen fluoride (HF) and from about 20 to about 98 wt. % 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd), based on the combined weight of the hydrogen fluoride (HF) and 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd).
5. The composition of claim 1 , wherein the composition has a boiling point of about −10° C.±0.5° C. at a pressure of about 7 psia±1 psia.
6. A method of forming an azeotropic or azeotrope-like composition comprising forming a blend consisting essentially of from about 1 to about 99 wt. % hydrogen fluoride (HF) and from about 1 to about 99 wt. % 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd), based on the combined weight of the hydrogen fluoride (HF) and 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd).
7. The method of claim 6 , wherein said forming step comprises forming a blend consisting of from about 2 to about 99 wt. % hydrogen fluoride (HF) and from about 1 to about 98 wt. % 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd), based on the combined weight of the hydrogen fluoride (HF) and 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd).
8. The method of claim 6 , wherein said forming step comprises forming a blend consisting of from about 2 to about 80 wt. % hydrogen fluoride (HF) and from about 20 to about 98 wt. % 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd), based on the combined weight of the hydrogen fluoride (HF) and 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd).
9. The method of claim 6 , wherein the composition has a boiling point of about −10° C.±0.5° C. at a pressure of about 7 psia±1 psia.
10. A method for fluorinating an organic compound comprising:
providing an azeotropic or azeotrope-like composition consisting of 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd) and hydrogen fluoride (HF); and
reacting at least a portion of said 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd) in the vapor phase with a fluorinating agent to produce at least one fluorinated organic compound.
11. The method of claim 10 , wherein said reacting step further comprises reacting at least a portion of said 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd) in the vapor phase with a fluorinating agent to produce 1-chloro-3,3,3-trifluoropropene (HCFO-1233zd).
12. The method of claim 10 , wherein said reacting step further comprises reacting at least a portion of said 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd) in the vapor phase with a fluorinating agent to produce 1,1,1,3,3,-pentafluoropropane (HFC-245fa).
13. The method of claim 10 , wherein said reacting step further comprises reacting at least a portion of said 1,3-dichloro-3,3-difluoroprop-1-ene (HCFO-1232zd) in the vapor phase with a fluorinating agent to produce 1,3,3,3-tetrafluoropropene (HFO-1234ze).