Patent classifications
C07C29/124
Methods and systems to form propylene chlorohydrin from dichloropropane using Lewis acid
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of dichloropropane in presence of Lewis acid and to further form propylene oxide from the propylene chlorohydrin.
Methods and systems to form propylene chlorohydrin from dichloropropane using Lewis acid
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of dichloropropane in presence of Lewis acid and to further form propylene oxide from the propylene chlorohydrin.
METHODS AND SYSTEMS TO FORM PROPYLENE CHLOROHYDRIN FROM DICHLOROPROPANE USING LEWIS ACID
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of dichloropropane in presence of Lewis acid and to further form propylene oxide from the propylene chlorohydrin.
METHODS AND SYSTEMS TO FORM PROPYLENE CHLOROHYDRIN FROM DICHLOROPROPANE USING LEWIS ACID
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of dichloropropane in presence of Lewis acid and to further form propylene oxide from the propylene chlorohydrin.
1-HALOALKADIENE AND A PROCESS FOR PREPARING THE SAME AND A PROCESS FOR PREPARING (9e, 11z)-9,11-HEXADECADIENYL ACETATE
A process to prepare (9E,11Z)-9,11-hexadecadienyl acetate with a good yield and high purity of the general formula (1): CH.sub.3(CH.sub.2).sub.3CHCHCHCH(CH.sub.2).sub.aX.=The process includes a step of conducting a Wittig reaction between a haloalkenal of the general formula (2): OHCCHCH(CH.sub.2).sub.aX, and a triarylphosphonium pentylide of the general formula (3): CH.sub.3(CH.sub.2).sub.3CH.sup.P.sup.+Ar.sub.3, to obtain the 1-haloalkadiene, and the use of a (7E,9Z)-1-halo-7,9-tetradecadiene obtained by the process for a process of preparing (9E, 11Z)-9,11-hexadecadienyl acetate.
1-HALOALKADIENE AND A PROCESS FOR PREPARING THE SAME AND A PROCESS FOR PREPARING (9e, 11z)-9,11-HEXADECADIENYL ACETATE
A process to prepare (9E,11Z)-9,11-hexadecadienyl acetate with a good yield and high purity of the general formula (1): CH.sub.3(CH.sub.2).sub.3CHCHCHCH(CH.sub.2).sub.aX.=The process includes a step of conducting a Wittig reaction between a haloalkenal of the general formula (2): OHCCHCH(CH.sub.2).sub.aX, and a triarylphosphonium pentylide of the general formula (3): CH.sub.3(CH.sub.2).sub.3CH.sup.P.sup.+Ar.sub.3, to obtain the 1-haloalkadiene, and the use of a (7E,9Z)-1-halo-7,9-tetradecadiene obtained by the process for a process of preparing (9E, 11Z)-9,11-hexadecadienyl acetate.
COMPOSITION COMPRISING 1-CHLORO-2,2-DIFLUOROETHANE
Compositions including 1-chloro-2,2-difluoroethane, and the uses thereof. A composition including 1-chloro-2,2-difluoroethane and at least one additional compound selected from 1,1-difluoroethylene, 1,1,1-trifluoroethane, chlorotrifluoroethylene, 1-chloro-1-fluoroethylene, 1,1-difluoroethane, trans-1-chloro-2-fluoroethylene, 1-chloro-2,2,2-trifluoroethane, 1-chloro-1,2,2-trifluoroethane, cis-1-chloro-2-fluoroethylene, 2,2-dichloro-1,1,1-trifluoroethane, 1,1-dichloro-1-fluoroethane, 1,1-dichloroethylene, 1,2-dichloro-1-fluoroethylene, 1,1-dichloro-2-fluoroethylene, 1,2-dichloro-1,1-difluoroethane, 1,1-dichloro-2,2-difluoroethane, cis-1,2-dichloroethylene, 1,2,2-trichloro-1,1-difluoroethane, 1,1,1-trichloroethane, 1,1-dichloroethane, 1,1,2-trichloro-1-fluoroethane, trichloroethylene, 1,1,2-trichloro-2-fluoroethane, 1,1,2-trichloroethane, 1,1,2,2-tetrachloro-1-fluoroethane, tetrachloroethylene, 1,1,1,2-tetrachloroethane, 1,1,2,2-tetrachloroethane, 1,1,1,2,2-pentachloroethane, tetrachloromethane, 1,2,2-trichloro-1-fluoroethylene, isomers of chloropropene, 1,2-dichloro-1-fluoroethylene, 1-chloro-2-fluoroethane, 1-chloro-1-fluoroethane, 1,1-chloro-2,2,2-trifluoroethane, 1,1,1-trichloro-2,2-difluoroethane, 1-chloroethylene, 1-fluoroethylene, H.sub.2O and HCl; the composition including at least 30% by weight of 1-chloro-2,2-difluoroethane, based on the total weight of the composition.
COMPOSITION COMPRISING 1-CHLORO-2,2-DIFLUOROETHANE
Compositions including 1-chloro-2,2-difluoroethane, and the uses thereof. A composition including 1-chloro-2,2-difluoroethane and at least one additional compound selected from 1,1-difluoroethylene, 1,1,1-trifluoroethane, chlorotrifluoroethylene, 1-chloro-1-fluoroethylene, 1,1-difluoroethane, trans-1-chloro-2-fluoroethylene, 1-chloro-2,2,2-trifluoroethane, 1-chloro-1,2,2-trifluoroethane, cis-1-chloro-2-fluoroethylene, 2,2-dichloro-1,1,1-trifluoroethane, 1,1-dichloro-1-fluoroethane, 1,1-dichloroethylene, 1,2-dichloro-1-fluoroethylene, 1,1-dichloro-2-fluoroethylene, 1,2-dichloro-1,1-difluoroethane, 1,1-dichloro-2,2-difluoroethane, cis-1,2-dichloroethylene, 1,2,2-trichloro-1,1-difluoroethane, 1,1,1-trichloroethane, 1,1-dichloroethane, 1,1,2-trichloro-1-fluoroethane, trichloroethylene, 1,1,2-trichloro-2-fluoroethane, 1,1,2-trichloroethane, 1,1,2,2-tetrachloro-1-fluoroethane, tetrachloroethylene, 1,1,1,2-tetrachloroethane, 1,1,2,2-tetrachloroethane, 1,1,1,2,2-pentachloroethane, tetrachloromethane, 1,2,2-trichloro-1-fluoroethylene, isomers of chloropropene, 1,2-dichloro-1-fluoroethylene, 1-chloro-2-fluoroethane, 1-chloro-1-fluoroethane, 1,1-chloro-2,2,2-trifluoroethane, 1,1,1-trichloro-2,2-difluoroethane, 1-chloroethylene, 1-fluoroethylene, H.sub.2O and HCl; the composition including at least 30% by weight of 1-chloro-2,2-difluoroethane, based on the total weight of the composition.
METHODS AND SYSTEMS TO FORM PROPYLENE CHLOROHYDRIN AND PROPYLENE OXIDE
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of 1,2-dichloropropane and to further form propylene oxide from propylene chlorohydrin.
METHODS AND SYSTEMS TO FORM PROPYLENE CHLOROHYDRIN AND PROPYLENE OXIDE
There are provided methods and systems to form propylene chlorohydrin by hydrolysis of 1,2-dichloropropane and to further form propylene oxide from propylene chlorohydrin.