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The preparation of 5‐(2‐bromoethyl)‐2‐iminooxazolidines via the von braun cyanogen bromide reaction
Author(s) -
Fielden Marvel L.
Publication year - 1973
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570100523
Subject(s) - chemistry , cyanogen bromide , bromide , organic chemistry , biochemistry , peptide sequence , gene
The reaction of certain 1‐alkyl‐3‐pyrrolidinols with cyanogen bromide in ether solution produced 3‐alkyl‐5‐(2‐bromoethyl)‐2‐iminooxazolidines. 5‐(2‐Bromoethyl)‐2‐ethyl‐2‐imino‐5‐phenyloxazolidine was tested for and found devoid of anorectic activity.
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