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Chemical transformations of 1,1-dichloro-2,2-diarylethanes

Journal Article · · Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States)
DOI:https://doi.org/10.1007/BF00956628· OSTI ID:6417439

Upon alkaline dehydrochlorination in diethyleneglycol, 1,1-dichloro-2,2-bis(p-chloro-phenyl)ethane (DDD) and its analogs are converted to diarylmethanes. Mo(CO)/sub 6/ catalyzes the intramolecular rearrangement of DDD and the dehydrochlorination of the product, 1,2-bis(4-chlorophenyl)-1,2-dichloroethane to 1-chloro-1,2-bis(4-chloro-phenyl)ethylene. A two-step procedure was proposed for the synthesis of 1,2-diarylacetylenes involving dehydrochlorination of DDD compounds by the action of Mo(CO)/sub 6/ to give 1-chloro-1,2-diarylethylenes and their subsequent alkaline dehydrochlorination.

Research Organization:
A.N. Nesmeyanov Institute of Heteroorganic Compounds, Moscow, USSR
OSTI ID:
6417439
Journal Information:
Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States), Journal Name: Bull. Acad. Sci. USSR, Div. Chem. Sci. (Engl. Transl.); (United States) Vol. 35:6; ISSN BACCA
Country of Publication:
United States
Language:
English