IP Library Granted Patent US 10,676,414
Granted Patent B2
US 10,676,414 · App. 15/681,972 · Granted Jun 9, 2020

Process for the manufacture of 1,1,1,3,3-pentachloropropane

Inventors: Hsueh Sung Tung (Getzville, NY); Ian Shankland (Randolph, NJ)
Assignee: Honeywell International Inc.
C07C17/00C07C17/206C07C17/275C07C17/278C07C19/01C07C19/08C07C21/18
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Quick Facts
Patent No.
US 10,676,414
App. No.
15/681,972
Granted
Jun 9, 2020
Kind
B2
Abstract

A process for the manufacture of haloalkanes, or more particularly to a process for the manufacture of 1,1,1,3,3-pentachloropropane (HCC-240fa) and/or 1,1,1,3-tetrachloropropane (HCC-250fb). The process includes (a) mixing a catalyst, co-catalyst and a haloalkane starting material under conditions suitable to produce a homogeneous mixture; (b) reacting the homogeneous mixture with a haloalkene and/or alkene starting material under conditions suitable to produce a haloalkane product stream; and (c) recovering a haloalkane product from said product stream.

Claims (36)

1. A process for preparing a haloalkane comprising:

(a) preparing a solid-free mixture comprising a catalyst, carbon tetrachloride, and vinyl chloride;

(b) reacting the solid-free mixture under conditions suitable to produce a haloalkane product stream;

(c) recovering 1,1,1,3,3-pentachloropropane from said product stream; and

(d) reacting said 1,1,1,3,3-pentachloropropane with hydrogen fluoride under conditions sufficient to yield 1,1,1,3,3-pentafluoropropane; and

wherein the process is a continuous process.

2. The process of claim 1 wherein said catalyst comprises CuCl and said co-catalyst comprises CH 3 CN, t-Bu-NH 2 , n-Bu-NH 2 , ethanol-amine, pyridine, sec-Bu-NH 2 , benzyl-NH 2 , n-Bu 3 N or combinations thereof.

3. The process of claim 1 wherein said catalyst comprises metallic Fe and said co-catalyst comprises hexamethylphosphoramide, (BuO) 3 P, (ClCH 2 CH 2 O) 3 P, tributlyphosphate, triphenylphosphate, (PhO) 3 P or combinations thereof.

4. The process of claim 1 wherein said haloalkane starting material has the formula C n H m X p wherein X is a halogen and wherein n is an integer from 1 to 200, and m and p are each independently 0 to 2n+2 provided that m+p=2 n+2.

5. The process of claim 1 wherein said haloalkene starting material has the formula C n H y X z wherein X is a halogen and wherein n is an integer from 2 to 200, and y and z are each independently 0 to 2 n provided that y+z=2 n.

6. The process of claim 1 wherein the product stream comprises a portion of said catalyst and a portion of said co-catalyst, and said process further comprises recovering and recycling said catalyst and said co-catalyst from said product stream.

7. The process of claim 6 wherein said catalyst and said co-catalyst are recovered and recycled as a mixture of the catalyst and co-catalyst.

8. The process of claim 1 wherein said catalyst comprises iron and said co-catalyst comprises tributlyphosphate.

9. A process for preparing a haloalkane, comprising the steps of:

(a) preparing a solid-free mixture comprising a catalyst, co-catalyst and a haloalkane starting material;

(b) reacting the solid-free mixture with a haloalkene starting material, an alkene starting material or both a haloalkene starting material and an alkene starting material under conditions suitable to produce a haloalkane product stream comprising 1, 1, 1, 3, 3-pentachloropropane;

(c) flash-distilling the haloalkane product stream of step (b) to separate a haloalkane product comprising 1, 1, 1, 3, 3-pentachloropropane, unreacted haloalkane starting material and unreacted haloalkene starting material from a mixture of said catalyst and co-catalyst; and

(d) recycling the catalyst and co-catalyst mixture to step (a);

wherein the process is a continuous process.

10. The process of claim 9 wherein said haloalkane product comprises 1,1,1,3,3-pentachloropropane, 1,1,1,3-tetrachloropropane, 1,1,1,3,3-pentachlorobutane or a combination thereof.

11. The process of claim 9 wherein said catalyst comprises iron and said co-catalyst comprises tributlyphosphate.

12. A process for preparing 1,1,1,3,3-pentafluoropropane and/or a combination of 1,1,1,3-tetrachloropropane and 3,3,3-trifluoro-1-propene comprising:

(a) preparing a solid-free mixture comprising a catalyst, co-catalyst and a haloalkane starting material;

(b) reacting the solid-free mixture with a haloalkene starting material and/or alkene starting material under conditions suitable to produce a 1,1,1,3,3-pentachloropropane product stream;

(c) recovering 1,1,1,3,3-pentachloropropane from said product stream; and

(d) reacting said 1,1,1,3,3-pentachloropropane with hydrogen fluoride under conditions sufficient to yield 1,1,1,3,3-pentafluoropropane;

wherein the process is a continuous process.

13. The process of claim 12 wherein said haloalkene starting material comprises vinyl chloride, 2-chloro-1-propene or a combination thereof.

14. The process of claim 12 wherein said alkene starting material comprises ethylene.

15. The process of claim 12 wherein said catalyst comprises CuCl and said co-catalyst comprises CH 3 CN, t-Bu-NH 2 , n-Bu-NH 2 , ethanol-amine, pyridine, sec-Bu-NH 2 , benzyl-NH 2 , n-Bu 3 N or combinations thereof.

16. The process of claim 12 wherein said catalyst comprises metallic Fe and said co-catalyst comprises hexamethylphosphoramide, (BuO) 3 P, (ClCH 2 CH 2 O) 3 P, tributlyphosphate, triphenylphosphate, (Pho) 3 P or combinations thereof.

17. The process of claim 12 wherein said haloalkane product is recovered from said product stream by flash-distillation.

18. The process of claim 12 wherein the product stream comprises a portion of said catalyst and a portion of said co-catalyst, and said process further comprises recovering and recycling said catalyst and said co-catalyst from said product stream.

19. The process of claim 18 wherein said catalyst and said co-catalyst are recovered and recycled as a mixture of the catalyst and co-catalyst.

20. The process of claim 12 , wherein said haloalkane starting material comprises carbon tetrachloride.

21. The process of claim 12 wherein said catalyst comprises iron and said co-catalyst comprises tributlyphosphate.

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 Mar 4, 2025
From: SHANKLAND, IAN; TUNG, HSUEH SUNG
To: HONEYWELL INTERNATIONAL INC.
Reel/Frame 070399/0205 →
Continuity (3)
Continuation 11869274 · Oct 9, 2007
Provisional Application 60850910 · Oct 11, 2006
Related Publication 20180127337A1 · May 10, 2018