The patent badge is an abbreviated version of the USPTO patent document. The patent badge does contain a link to the full patent document.

The patent badge is an abbreviated version of the USPTO patent document. The patent badge covers the following: Patent number, Date patent was issued, Date patent was filed, Title of the patent, Applicant, Inventor, Assignee, Attorney firm, Primary examiner, Assistant examiner, CPCs, and Abstract. The patent badge does contain a link to the full patent document (in Adobe Acrobat format, aka pdf). To download or print any patent click here.

Date of Patent:
Dec. 27, 2011

Filed:

Jan. 03, 2007
Applicants:

Hsueh S. Tung, Getzville, NY (US);

Sudip Mukhopadhyay, Williamsville, NY (US);

Michael Van Der Puy, Amherst, NY (US);

Daniel C. Merkel, West Seneca, NY (US);

Jing Ji MA, West Seneca, NY (US);

Cheryl L. Bortz, N. Tonawanda, NY (US);

Barbara A. Light, Niagara Falls, NY (US);

Steven D. Phillips, New York, NY (US);

Rajesh K. Dubey, Williamsville, NY (US);

Inventors:

Hsueh S. Tung, Getzville, NY (US);

Sudip Mukhopadhyay, Williamsville, NY (US);

Michael Van Der Puy, Amherst, NY (US);

Daniel C. Merkel, West Seneca, NY (US);

Jing Ji Ma, West Seneca, NY (US);

Cheryl L. Bortz, N. Tonawanda, NY (US);

Barbara A. Light, Niagara Falls, NY (US);

Steven D. Phillips, New York, NY (US);

Rajesh K. Dubey, Williamsville, NY (US);

Assignee:

Honeywell International, Inc., Morristown, NJ (US);

Attorney:
Primary Examiner:
Assistant Examiner:
Int. Cl.
CPC ...
C07C 17/00 (2006.01); C07C 19/08 (2006.01); C07C 21/18 (2006.01); C07C 23/00 (2006.01); C07C 25/13 (2006.01);
U.S. Cl.
CPC ...
Abstract

Disclosed are processes for the production of fluorinated olefins, preferably adapted to commercialization of CFCF═CH(1234yf). Three steps may be used in preferred embodiments in which a feedstock such as CCl═CClCHCl (which may be purchased or synthesized from 1,2,3-trichloropropane) is fluorinated (preferably with HF in gas-phase in the presence of a catalyst) to synthesize a compound such as CFCCl═CH, preferably in a 80-96% selectivity. The CFCCl═CHis preferably converted to CFCFClCH(244-isomer) using a SbClas the catalyst which is then transformed selectively to 1234yf, preferably in a gas-phase catalytic reaction using activated carbon as the catalyst. For the first step, a mixture of CrOand FeCl/C is preferably used as the catalyst to achieve high selectivity to CFCCl═CH(96%). In the second step, SbCl/C is preferably used as the selective catalyst for transforming 1233xf to 244-isomer, CFCFClCH. The intermediates are preferably isolated and purified by distillation and used in the next step without further purification, preferably to a purity level of greater than about 95%.


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