Process for the production of 1-chloro-3,3,3-trifluoropropene (HCFO-1233zd)

1. A process for the production of 1-chloro-3,3,3-trifluoropropene (HCFO-1233zd), comprising the steps of:

providing a reactant composition including 1,3,3-trichloro-1,1-difluoropropane (HCFC-242fa);

dehydrochlorinating the HCFC-242fa in the presence of a basic solution to form 1,3-dichloro-3,3-difluoropropene (HCFO-1232zd); and

fluorinating the HCFO-1232zd with hydrogen fluoride (HF) to produce HCFO-1233zd.

2. The process of claim 1 wherein following said fluorinating step, the HCFO-1233zd produced is predominantly HCFO-1233zd(E).

3. The process of claim 1 , wherein said dehydrochlorinating step is performed at a temperature between 0° C. and 100° C.

4. The process of claim 1 , wherein said fluorinating step is performed at a temperature between 80° C. and 150° C.

5. The process of claim 1 , wherein said fluorinating step is performed in the absence of a catalyst.

6. The process of claim 1 , wherein the reactant composition further includes hydrogen fluoride (HF) and said process further includes the additional step, after said providing step and prior to said dehydrochlorinating step, of separating HF from the reactant composition.

7. The process of claim 1 , further comprising the additional step, after said dehydrochlorinating step and prior to said fluorinating step, of drying the HCFO-1232zd.

8. The process of claim 1 , wherein the basic solution in said dehydrochlorinating step is selected from the group consisting of potassium hydroxide (KOH), sodium hydroxide (NaOH), and calcium hydroxide (CaOH).

9. A process for the production of 1-chloro-3,3,3-trifluoropropene (HCFO-1233zd), comprising the steps of:

fluorinating 1,1,1,3,3-pentachloropropane (HCC-240fa) with hydrofluoric acid (HF) to produce a product stream including HCFO-1233zd and 1,3,3-trichloro-1,1-difluoropropane (HCFC-242fa);

separating HCFC-242fa from the product stream;

dehydrochlorinating the HCFC-242fa in a liquid phase in the presence of a basic solution to form 1,3-dichloro-3,3-difluoropropene (HCFO-1232zd); and

fluorinating the HCFO-1232zd with hydrogen fluoride (HF) to produce HCFO-1233zd.

10. The process of claim 9 , wherein said first fluorinating step is performed at a reaction temperature between 120° C. and 140° C. and at a reaction pressure of between 230 psig and 400 psig.

11. The process of claim 9 wherein, following said second fluorinating step, the HCFO-1233zd produced is predominantly HCFO-1233zd(E).

12. The process of claim 9 , wherein said dehydrochlorinating step is performed at a temperature between 0° C. and 100° C.

13. The process of claim 9 , wherein said second fluorinating step is performed at a temperature between 80° C. and 150° C.

14. The process of claim 9 , wherein said second fluorinating step is performed in the absence of a catalyst.

15. The process of claim 9 , wherein said process further includes an additional step, after said first fluorinating step and prior to said separating step, of separating HF from the product stream.

16. The process of claim 9 , further comprising the additional step, after said dehydrochlorinating step and prior to said second fluorinating step, of drying the HCFO-1232zd.

17. The process of claim 9 , further comprising the additional step, after said second fluorinating step, of recycling at least one of unreacted HCFO-1232zd and unreacted HF back to said first fluorinating step.

18. The process of claim 9 , wherein said separating step is conducted via vacuum distillation.

19. The process of claim 9 , wherein said separating step is conducted via distillation at a pressure between 10 torr and 5,200 torr.