IP Library Granted Patent US 8,835,698
Granted Patent B2
US 8,835,698 · App. 13/888,443 · Granted Sep 16, 2014

Method for producing fluorinated organic compounds

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Quick Facts
Patent No.
US 8,835,698
App. No.
13/888,443
Granted
Sep 16, 2014
Kind
B2
Abstract

Disclosed are processes for the production of fluorinated olefins, preferably adapted to commercialization of CF 3 CF═CH 2 (1234yf). In certain preferred embodiments the processes comprise first exposing a compound of Formula (IA) C(X) 2 ═CClC(X) 3   (IA) where each X is independently F, Cl or H, preferably CCl 2 ═CClCH 2 Cl, to one or more sets of reaction conditions, but preferably a substantially single set of reaction conditions, effective to produce at least one chlorofluoropropane, preferably in accordance with Formula (IB): CF 3 CClX′C(X′) 3   Formula (IB) where each X′ is independently F, Cl or H, and then exposing the compound of Formula (IB) to one or more sets of reaction conditions, but preferably a substantially single set of reaction conditions, effective to produce a compound of Formula (II) CF 3 CF═CHZ  (II) where Z is H, F, Cl, I or Br.

Claims (17)

1. A process for making a tetrafluoropropene, comprising:

dehydrohalogenating 2-chloro-1,1,1,2-tetrafluoropropane (HCFC-244bb) in the presence of a caustic agent.

2. The process of claim 1 wherein the tetrafluoropropene is 2,3,3,3-tetrafluoropropene.

3. The process of claim 1 wherein the caustic agent is at least one agent selected from the group consisting of KOH, NaOH, Ca(OH) 2 , and CaO.

4. The process of claim 3 wherein the caustic agent is KOH.

5. The process of claim 1 wherein the caustic agent is provided in a solution having a caustic agent strength of between about 2 wt % and about 100 wt. %.

6. The process of claim 1 wherein the caustic agent is provided in a solution having a caustic agent strength of between about 5 wt % and about 90 wt. %.

7. The process of claim 1 wherein the caustic agent is provided in a solution having a caustic agent strength of between about 10 wt % and about 80 wt. %.

8. The process of claim 1 wherein a mole ratio of the caustic agent:HCFC-244bb is from about 1:1 to about 2:1.

9. The process of claim 1 wherein a mole ratio of caustic agent:HCFC-244bb is from about 1.1:1 to about 1.5:1.

10. The process of claim 1 wherein a mole ratio of caustic agent:HCFC-244bb is from about 1.2:1 to about 1.4:1.

11. The process of claim 1 wherein the dehydrohalogenating step is conducted at a temperature from about 20° C. to about 100° C.

12. The process of claim 1 wherein the dehydrohalogenating step is conducted at a temperature from about 30° C. to about 90° C.

13. The process of claim 1 wherein the dehydrohalogenating step is conducted at a temperature from about 40° C. to about 80° C.

14. The process of claim 1 wherein a reaction pressure of the process ranges from atmospheric pressure, super-atmospheric pressure and sub-atmospheric pressure.

15. The process of claim 1 further comprising a phase transfer catalyst.

16. The process of claim 1 further comprising recovering the tetrafluoropropene.

Assignments (2)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 7, 2013
From: JOHNSON, ROBERT C.; TUNG, HSUEH S.; MERKEL, DANIEL C.
To: HONEYWELL INTERNATIONAL INC.
Reel/Frame 030360/0890 →