IP Library Patent Application 19301918
Patent Application
App. No. 19/301,918

PROCESS FOR CATALYTIC CONVERSION OF MIXTURES OF HCFO-1233zd(Z) AND HCFC-244fa INTO HCFO-1233zd(E)

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Patent No.
US None
App. No.
19/301,918
Abstract

A method for conversion of a composition containing HCFO-1233zd(Z) and HCFC-244fa to form HCFO-1233zd(E) by reacting a mixture including HCFO-1233zd(Z) and HCFC-244fa in a vapor phase in the presence of a catalyst to simultaneously isomerize HCFO-1233zd(Z) to form HCFO-1233zd(E) and dehydrohalogenate HCFC-244fa to form HCFO-1233zd(E). The catalyst may be a chromium-based catalyst such as chromium trifluoride, chromium oxyfluoride, or chromium oxide, for example.

Claims (21)

1 . A method for the simultaneous conversion of a composition containing HCFO-1233zd(Z) and HCFC-244fa to form HCFO-1233zd(E), comprising the steps of:

providing a composition including HCFO-1233zd(Z) and HCFC-244fa; and

reacting the composition in a vapor phase in a reactor in the presence of a chromium trifluoride (CrF 3 ) catalyst to simultaneously isomerize HCFO-1233zd(Z) to form HCFO-1233zd(E) and dehydrohalogenate HCFC-244fa to form HCFO-1233zd(E).

2 . The method of claim 1 , wherein the reacting step is conducted at a temperature between 80° C. and 250° C.

3 . The method of claim 2 , wherein the reacting step is conducted at a temperature between 100° C. and 200° C.

4 . The method of claim 1 , wherein a contact time between the composition and the catalyst is between 1 second and 150 seconds.

5 . The method of claim 4 , wherein a contact time between the composition and the catalyst is between 25 seconds and 125 seconds.

6 . The method of claim 1 , wherein a pressure in the reactor is between 25 psig and 100 psig.

7 . The method of claim 1 , wherein during the reacting step, the reactor includes less than 50 ppm water.

8 . The method of claim 1 , wherein the reacting step achieves a conversion of HCFO-1233zd(Z) to HCFO-1233zd(E) between 88% and 96%.

9 . The method of claim 1 , wherein the reacting step achieves a conversion of HCFC-244fa to HCFO-1233zd(E) between 90% and 99%.

10 . The method of claim 1 , wherein the reacting step achieves a selectivity to HCFO-1233zd(E) between 90% and 97%.

11 . The method of claim 1 , wherein in the providing step, total impurities are present in an amount less than 10 wt. %, based on the total weight of the composition.

12 . The method of claim 1 , wherein in the providing step, total impurities are present in an amount less than 6 wt. %, based on the total weight of the composition.

13 . The method of claim 1 , wherein in the providing step, total impurities are present in an amount less than 1.5 wt. %, based on the total weight of the composition.

14 . The method of claim 1 , wherein any HCFC-243fa and HCFC-243 db, if present in the composition, is present in an amount less than 3 wt. % based on the total weight of the composition.

15 . The method of claim 1 , further comprising, after the reacting step, the additional steps of:

distilling the composition in a distillation column;

removing an overhead stream from the distillation column, the overhead stream concentrated in HCFO-1233zd(E); and

removing a bottoms stream from the distillation column, the bottoms stream concentrated in HCFO-1233zd(Z) and HCFC-244fa.

16 . The method of claim 15 , further comprising, after the second removing step, the additional step of recycling the bottoms stream back to the reactor.

Assignments (1)
SECURITY INTEREST Recorded Jan 12, 2026
From: SOLSTICE ADVANCED MATERIALS US, INC.
To: JPMORGAN CHASE BANK, N.A., AS ADMINISTRATIVE AGENT
Reel/Frame 074569/0260 →