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1,2,2-Trichlorovinylamines

Reaction of 7V,A-diethyl-2,2,2-trichloroacetamide with trialkyl phosphites or triphenylphosphine to give N, N-diethyl-1,2,2-trichlorovinylamine [152-154],... [Pg.64]

N,N-Diethyl-1,2,2-trichlorovinylamine has been prepared by the action of trimethyl, triethyl, or triisopropyl phosphite or triphenylphosphine on N,N-diethyl-2,2,2-trichloroacetamide., These methods require a reaction temperature of 150-160° and several distillations in order to obtain a pure product. Consequently, the yields of the vinylamine are lower than by the present procedure.3... [Pg.23]

E pic hi orh yd rin 2-Chlorodioxene 2,A-Dinitrofluorobenzene co-Tribromo-acetophenone lodobenzene dichloride CICN, BrCN, ICn CHFCICF2N(C2Hs)2 N-Diethyl-1,2,2-trichlorovinylamine N-Chlorodiethylamine ICH2CONH2 Bromocyanoacetamide T richloroacetamides Dibromomalonamide a,fi-Dibromopropionitrile CClgCN... [Pg.286]

CHFCICF N(C H,) N,N-Diethyl-1,2,2-trichlorovinylamine N-Chlorodiethylamine ClsC-N=CCl (tri-chloromethy lisocyanide dichloride) Hydroximinohalides, C H,C( NOH)Cl ICH CONH Bromocyanoacetamide T richloroacetamides Dibromomalonamide a,fi-Dibromopropio-nitrile, CBr iCN), CClsCN... [Pg.286]


See other pages where 1,2,2-Trichlorovinylamines is mentioned: [Pg.708]    [Pg.532]    [Pg.558]    [Pg.319]    [Pg.749]    [Pg.251]    [Pg.520]    [Pg.596]    [Pg.300]    [Pg.308]    [Pg.535]    [Pg.692]    [Pg.508]    [Pg.244]    [Pg.481]    [Pg.142]    [Pg.614]   


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1,2,2-Trichlorovinylamines trichloroacetamides

N-Diethyl-1,2,2-trichlorovinylamine

Thioacetamides, trichlorosynthesis via thiolysis of trichlorovinylamines

Trichlorovinylamines, chlorination

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