136661-37-5Relevant articles and documents
TRANSFORMATIONS OF 1,1,1-TRICHLORO-2,2-BIS(4-CHLOROPHENYL)ETHANE, 4,4'-DICHLOROBENZOPHENONE, AND THEIR NITRO DERIVATIVES IN A SODIUM HYDROXIDE-AMIDE SOLVENT MEDIUM
Sibrikov, S. G.,Kazin, V. N.,Kopeikin, V. V.,Mironov, G. S.,Orlova, T. N.
, p. 325 - 327 (2007/10/02)
The reaction of 1,1,1-trichloro-2,2-bis(4-chlorophenyl)ethane with alkali in an amide solvent leads to dehydrochlorination of the substrate.In 1,1,1-trichloro-2,2-bis(3-nitro-4-chlorophenyl)ethane under the same conditions substitution of the chlorine atoms in the bridging group by dimethylamino groups, formed as a result of hydrolysis of the solvent, occurs after dehydrochlorination.In 1,1,1-trichloro-2,2-bis(3,5-dinitro-4-chlorophenyl)ethane the chlorine atoms of benzene ring are substituted by dimethylamino groups.In the presence of CuCl 4,4'-dichlorobenzophenone is converted into 4,4'-bis(dimethylamino)benzophenone. 3,3'-Dinitro-4,4'-dichlorobenzophenone reacts with the sodium hydroxide-amide solvent system with the formation of 3,3'-dinitro-4,4'-bis(dimethylamino)-benzophenone and 3,3'-dinitro-4-hydroxy-4'-dimethylaminobenzophenone, the ratio of which is determined by the reaction temperature.