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Title: Epoxidation of propylene dimers and isomerization of mixtures obtained

Journal Article · · J. Appl. Chem. USSR (Engl. Transl.); (United States)
OSTI ID:6180767

Mixtures of hexenes are obtained in the dimerization of propylene on a Ziegler catalyst. By the epoxidation of this mixture by organic peroxides, followed by isomerization of the oxides, C/sub 6/ ketones, which are used as solvents, can be obtained. The hexenes were obtained by dimerization of propylene in the presence of a Ni(C/sub 5/H/sub 7/O/sub 2/)/sub 2/-P(C/sub 6/H/sub 5/)/sub 3/-(C/sub 3/H/sub 5/)/sub 2/AlCl catalytic system. The epoxidation was carried with technical grade isopropylbenzyl hydroperoxide (IPBHP). MoO/sub 2/(C/sub 5/H/sub 7/O/sub 2/)/sub 2/ was used as the catalyst. The relative rates of epoxidation of different isomers contained in the dimeric fraction, with respect to 2-methyl-1-pentene, was determined by means of competing reactions.

OSTI ID:
6180767
Journal Information:
J. Appl. Chem. USSR (Engl. Transl.); (United States), Vol. 60:11; Other Information: Translated from Zh. Prikl. Khim.; 60: No. 11, 2593-2595(Nov 1987)
Country of Publication:
United States
Language:
English