Author:
Cremlyn RJ,Cronje T,Goulding K
Abstract
Phenoxybenzene (diphenyl
ether) has been converted into the 4-sulfonyl chloride (1) which on condensation
with various nucleophilic reagents gave a range of sulfonyl derivatives (2-11),
such as the azide, hydrazides, and hydrazones. The sulfonyl chloride (1), by
nitration, gave 4-(4'-nitrophenoxy)benzenesulfonyl chloride (12) which was
similarly converted into sulfonyl derivatives (13-18). Reaction of o-chlorophenol with p-chloronitrobenzene afforded 2-chlorophenyl 4-nitrophenyl ether;
with chlorosulfonic acid this gave the sulfonyl chloride (19) which was
converted into the sulfonyl derivatives (20)-(25). Condensation of
2,6-dichlorophenol with p-chloronitrobenzene
similarly gave the substituted diphenyl ether (26) which with chlorosulfonic
acid afforded 3,5- dichloro-4-(4'-nitrophenoxy)benzenesulfonyl chloride (27).
The phenoxybenzenesulfonyl derivatives are of interest as potential herbicides
and their algicidal and antibacterial properties are briefly discussed.
Cited by
12 articles.
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