Process for the preparation of 2,3,3,3-tetrafluoropropene (HFO-1234yf)
View Patent ↗A process for the preparation of 2,3,3,3-tetrafluoropropene (HFO-1234yf). HFO-1234yf is a refrigerant with low global warming potential. A process comprises a) reacting chlorotrifluoroethylene with a methyl halide to form an intermediate product stream; and b) reacting the intermediate product stream with hydrogen fluoride to thereby produce a result comprising 2,3,3,3-tetrafluoropropene.
1. A process for the preparation of 2,3,3,3-tetrafluoropropene which comprises:
a) reacting chlorotrifluoroethylene with a methyl halide to form an intermediate product stream; and
b) reacting the intermediate product stream with hydrogen fluoride to thereby produce a result comprising 2,3,3,3-tetrafluoropropene, wherein the reacting of the intermediate product stream with hydrogen fluoride is conducted in the presence of a fluorination catalyst comprising at least one of activated carbon, activated carbon impregnated with metal salts, chromium oxide, and fluorinated chromium oxide.
2. The process of claim 1 comprising the subsequent step of separating 2,3,3,3-tetrafluoropropene from the result.
3. The process of claim 1 comprising the subsequent step of separating 2,3,3,3-tetrafluoropropene from the result by distillation.
4. The process of claim 1 wherein the methyl halide comprises methyl chloride.
5. The process of claim 1 wherein step a) is conducted in a first reactor and then step b) is conducted in a second reactor.
6. The process of claim 1 wherein steps a) and b) are conducted in a vapor phase.
7. The process of claim 1 wherein step a) is conducted at a temperature of from about 500° C. to about 1000° C.
8. The process of claim 1 wherein step a) is conducted at a temperature of from about 600° C. to about 900° C.
9. The process of claim 1 wherein step a) is conducted at a temperature of from about 650° C. to about 750° C.
10. The process of claim 1 wherein the mole ratio of chlorotrifluoroethylene methyl halide in step a) ranges from about 0.7 to about 1.5.
11. The process of claim 1 wherein the mole ratio of chlorotrifluoroethylene methyl halide in step a) ranges from about 0.9 to about 1.1.
12. The process of claim 1 wherein the contact time between the chlorotrifluoroethylene and the methyl halide in step a) ranges from more than 0 seconds to about five seconds.
13. The process of claim 1 wherein the contact time between the chlorotrifluoroethylene and the methyl halide in step a) ranges from about 0.5 second to about 3 seconds.
14. The process of claim 1 wherein the reacting of the intermediate product stream with hydrogen fluoride is conducted in the presence of a fluorination catalyst.
15. The process of claim 1 wherein the reacting of the intermediate product stream with hydrogen fluoride is conducted in the presence of a fluorination catalyst comprising chromium oxide.
16. The process of claim 1 wherein the reacting of the intermediate product stream with hydrogen fluoride is conducted with at least one mole of hydrogen fluoride per mole of chlorotrifluoroethylene from step a).
17. The process of claim 1 wherein the reacting of the intermediate product stream with hydrogen fluoride is conducted with from about one mole to about two moles of hydrogen fluoride per mole of chlorotrifluoroethylene from step a).
18. The process of claim 1 wherein the reacting of the intermediate product stream with hydrogen fluoride is conducted with from about one mole to about five moles of hydrogen fluoride per mole of chlorotrifluoroethylene from step a).
19. The process of claim 1 wherein step b) is conducted at a temperature of from about 225° C. to about 575° C.
20. The process of claim 1 wherein step b) is conducted at a temperature of from about 275° C. to about 560° C.
21. The process of claim 1 wherein step b) is conducted at a temperature of from about 280° C. to about 550° C.