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Formation of Heterocyclic and Polycyclic Compounds from Amino Alcohols and Dialdehydes
Author(s) -
Peera Asghar A.,
Tomlinson Ian A.
Publication year - 2015
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.2080
Subject(s) - chemistry , glyoxal , oxazolidine , organic chemistry , cyclohexane , condensation , bicyclic molecule , thermodynamics , physics
Amino alcohols typically react with aldehydes to produce oxazolidines. It was hypothesized that the condensation of several commercially available amino alcohols with dialdehydes would produce a series of bicyclic oxazolidines containing two secondary amines. However, there were remarkable differences in the type of products formed depending on the structure of the dicarbonyl compounds and the reaction conditions. When linear aliphatic dialdehydes such as glyoxal were used, the expected bis‐oxazolidines were not produced; instead, polycyclic structures or oxazines were formed. However, when cyclic dialdehydes such as 1,3/1,4 cyclohexane dicarboxaldehyde were used, they resulted in products bearing the desired oxazolidine moieties.