Patent classifications
C07C2527/12
Selective catalytic dehydrochlorination of hydrochlorofluorocarbons
A dehydrochlorination process is disclosed. The process involves contacting R.sub.fCHClCH.sub.2Cl with a chromium oxyfluoride catalyst in a reaction zone to produce a product mixture comprising R.sub.fCCl═CH.sub.2, wherein R.sub.f is a perfluorinated alkyl group.
HYDROFLUORINATION OF 1233XF TO 244BB BY SBF5
A method hydrofluorinates an olefin of the formula: RCX═CYZ to produce a hydrofluoroalkane of formula RCXFCHYZ or RCXHCFYZ, where X, Y, and Z are independently the same or different and are selected from the group consisting of H, F, Cl, Br, and C.sub.1-C.sub.6 alkyl which is partially or fully substituted with chloro or fluoro or bromo; and R is a C.sub.1-C.sub.6 alkyl which is unsubstituted or substituted with chloro or fluoro or bromo. The method includes reacting the olefin with HF in the vapor phase, in the presence of SbF.sub.5, at a temperature ranging from about −30° C. to about 65° C. and compositions formed by the process.
SELECTIVE CATALYTIC DEHYDROCHLORINATION OF HYDROCHLOROFLUOROCARBONS
A dehydrochlorination process is disclosed. The process involves contacting R.sub.fCHClCH.sub.2Cl with a chromium oxyfluoride catalyst in a reaction zone to produce a product mixture comprising R.sub.fCCl═CH.sub.2, wherein R.sub.f is a perfluorinated alkyl group.
HYDROFLUORINATION OF 1233XF TO 244BB BY SBF5
A method hydrofluorinates an olefin of the formula: RCX=CYZ to produce a hydrofluoroalkane of formula RCXFCHYZ or RCXHCFYZ, where X, Y, and Z are independently the same or different and are selected from the group consisting of H, F, Cl, Br, and C.sub.1-C.sub.6 alkyl which is partially or fully substituted with chloro or fluoro or bromo; and R is a C.sub.1-C.sub.6 alkyl which is unsubstituted or substituted with chloro or fluoro or bromo. The method includes reacting the olefin with HF in the vapor phase, in the presence of SbF.sub.5, at a temperature ranging from about −30° C. to about 65° C. and compositions formed by the process.
Hydrofluoroalkane composition
The disclosure relates to a method for hydrofluorination of an olefin of the formula: RCX═CYZ to produce a hydrofluoroalkane of formula RCXFCHYZ or RCXHCFYZ, wherein X, Y, and Z are independently the same or different and are selected from the group consisting of H, F, Cl, Br, and C.sub.1-C.sub.6 alkyl which is partially or fully substituted with chloro or fluoro or bromo; and R is a C.sub.1-C.sub.6 alkyl which is unsubstituted or substituted with chloro or fluoro or bromo, comprising reacting the olefin with HF in the liquid-phase, in the presence of SbF.sub.5, at a temperature ranging from about −30° C. to about 65° C. and compositions formed by the process.
Hydrofluoroalkane composition
The disclosure relates to a method for hydrofluorination of an olefin of the formula: RCX═CYZ to produce a hydrofluoroalkane of formula RCXFCHYZ or RCXHCFYZ, wherein X, Y, and Z are independently the same or different and are selected from the group consisting of H, F, Cl, Br, and C.sub.1-C.sub.6 alkyl which is partially or fully substituted with chloro or fluoro or bromo; and R is a C.sub.1-C.sub.6 alkyl which is unsubstituted or substituted with chloro or fluoro or bromo, comprising reacting the olefin with HF in the liquid-phase, in the presence of SbF.sub.5, at a temperature ranging from about −30° C. to about 65° C. and compositions formed by the process.
Methods for the preparation and use of suspensions of chemically-treated solid oxides in an olefin-derived liquid medium
The present invention discloses processes for oligomerizing an olefin feedstock containing C.sub.4 to C.sub.20 alpha olefins using a catalyst system containing a metallocene compound, an organoaluminum compound, and a suspension of a chemically-treated solid oxide. The liquid medium for the suspension of the chemically-treated solid oxide can be an alpha-olefin oligomer product formed by the oligomerization process.
HYDROFLUORINATION OF 1233XF TO 244BB BY SBF5
The disclosure relates to a method for hydrofluorination of an olefin of the formula: RCXCYZ to produce a hydrofluoroalkane of formula RCXFCHYZ or RCXHCFYZ, wherein X, Y, and Z are independently the same or different and are selected from the group consisting of H, F, Cl, Br, and C.sub.1-C.sub.6 alkyl which is partially or fully substituted with chloro or fluoro or bromo; and R is a C.sub.1-C.sub.6 alkyl which is unsubstituted or substituted with chloro or fluoro or bromo, comprising reacting the olefin with HF in the liquid-phase, in the presence of SbF.sub.5, at a temperature ranging from about 30 C. to about 65 C. and compositions formed by the process.
SELECTIVE CATALYTIC DEHYDROCHLORINATION OF HYDRCHLOROFLUOROCARBONS
A dehydrochlorination process is disclosed. The process involves contacting R.sub.fCHClCH.sub.2Cl with a chromium oxyfluoride catalyst in a reaction zone to produce a product mixture comprising R.sub.fCClCH.sub.2, wherein R.sub.f is a perfluorinated alkyl group.
Methods of Preparing an Aromatization Catalyst
Catalysts and method of preparing the catalysts are disclosed. One of the catalysts includes a zeolite support, a Group VIII metal on the zeolite support, and at least two halides bound to the zeolite support, to the Group VIII metal, or to both, and can have an average crush strength greater than 11.25 lb based on at least two samples of pellets of the catalyst measured in accordance with ASTM D4179.