Halogenated pyridines II. Reactions of 3‐halogenomethyl‐pyridines. The facile syntheis of 3‐halogenomethyl‐pyridines provides an easy access to a variety of new 2, 6‐di‐ and 2, 5, 6‐trihalogented pyridines with various functional groups in the 3‐position of the pyridine ring. Substitution reactions of the 3‐halogenomethyl groups, their Friedel Crafts reactions, and nitrations of the halogenated pyridine ring are reported.
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Horn et al. (1976) studied this question.
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