Patent classifications
C07C2527/12
Compositions including olefin and hydrofluoroalkane
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.
Hydrofluorination of a halogenated olefin with SbF5 in the liquid phase
The disclosure relates to a method for hydrofluorination of an olefin of the formula: RCX=CYZ to produce a hydrofluoroalkane of formula RCXFCHYZ or RCHXCFYZ, 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.
Method for producing aromatic compound
In a cross coupling reaction, in a case where a halogen atom is selected as the leaving group of the raw material compound, a harmful halogen waste forms as a by-product after the reaction, and disposal of the waste liquid is complicated and environmental burden is high. In a carbon-hydrogen activation cross coupling reaction which requires no halogen atom as the leaving group, although no halogen waste forms as a by-product, the reaction substrate is considerably restricted, and the reaction remains a limited molecular construction method. A method for producing an aromatic compound, which comprises subjecting an aromatic nitro compound and a boronic acid compound to a cross coupling reaction in the presence of a metal catalyst.
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.
OLEFIN OLIGOMERIZATIONS USING CHEMICALLY-TREATED SOLID OXIDES
Disclosed is a polyalphaolefin made up of hydrogenated oligomers. The oligomers include at least 80 wt. % of a C.sub.6 to C.sub.12 normal alpha olefin monomer. The polyalphaolefin has a viscosity index greater than or equal to 110 and a kinematic viscosity at 40 C. of less than or equal to 1750 cSt.
Olefin oligomerizations using chemically-treated solid oxides
The present invention discloses processes for oligomerizing a monomer containing C.sub.3 to C.sub.30 olefins using a chemically-treated solid oxide, such as fluorided silica-coated alumina and fluorided-chlorided silica-coated alumina.
Method for synthesizing dissymmetric sulfoether
A method for synthesizing dissymmetric sulfoether includes the following step: a) under the condition of tetrabutylammonium halide catalysis, compounds having a structure of formula (I), compounds having a structure of formula (II) and salts having sulfur and oxygen are reacted in a solvent to give dissymmetric sulfoether having a structure of formula (III).
PROCESS FOR PRODUCING AROMATICS, P-XYLENE AND TEREPHTHALIC ACID
The present invention relates to a process for producing aromatics, p-xylene and terephthalic acid. The process for producing aromatics comprises a step of contacting an oxygen-containing raw material with an aromatization catalyst, under aromatization reaction conditions, to produce aromatics. The process for producing aromatics has an advantage of high yield of carbon as aromatics.
PROCESS FOR MAKING TETRACHLOROPROPENE BY CATALYZED GAS-PHASE DEHYDROCHLORINATION OF PENTACHLOROPROPANE
The present disclosure relates to catalyzed gas-phase dehydrochlorination of a pentachloropropane to form a tetrachloropropene with high selectivity and purity.
Continuous mixing reactor and method of use
A continuous mixing reactor has an outer shell having a cylindrical portion with a central section and two opposite conical end sections; a circulation tube within the shell so that an annular passage forms between the shell and the circulation tube; an impeller within and positioned adjacent to one end of the circulation tube; and heat exchange means penetrating the outer shell and extending into the end of the circulation tube opposite the impeller. The outer shell has a hydraulic head forming one end of the shell, a heat exchange medium header at the opposite end of the shell. The circulation tube nearer the heat exchange medium header terminates at or downstream from a tangential plane extending through the shell at the intersection of the central section and the conical end section of the cylindrical portion of shell. The reactor is useful in an alkylation process.