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Chloral condensation with aromatic hydrocarbons

Chloral condensations with aromatic hydrocarbons (and related derivatives) give rise to diaryltrichloroethane compounds, and are brought about in the presence of acid catalysts, proceeding with the formation of carbinol intermediates (Scheme 2.1). Commonly used catalysts include concentrated H2SO4 and its monohydrate, HCl, HF, I O,-, Lewis acids and a series of other acid agents [1, 2]. [Pg.5]

Of numerous chloral condensations with aromatic hydrocarbons the most interesting for the synthesis of condensation monomers are the reactions with benzene [3], toluene [4], acenaphthene [5], phenol [6], anisol [7], acetanilide [8] and halobenzenes like chlorobenzene [9] and fluorobenzene [10]. In general terms, these reactions proceed according to Scheme 2.2 and give the desired 1,1,1-trichloro-... [Pg.5]

Hydrocarbons, aromatic, acylation, 317 alkylation, 2 carboxylation, 425 condensation with chloral, 297 condensation with ethylene oxide, 181... [Pg.442]


See other pages where Chloral condensation with aromatic hydrocarbons is mentioned: [Pg.591]    [Pg.600]   
See also in sourсe #XX -- [ Pg.5 , Pg.6 ]




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Chloral

Condensation aromatic

Condensed hydrocarbon

Hydrocarbon condensation

Hydrocarbons aromatization with

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