Open Access2‐(Cyclohexa‐1,4‐dienyl)acetic acid
Author(s) -
Therrien Bruno,
SüssFink Georg
Publication year - 2006
Publication title -
acta crystallographica section e
Language(s) - English
Resource type - Journals
ISSN - 1600-5368
DOI - 10.1107/s1600536806013158
Subject(s) - dimer , acetic acid , phenylacetic acid , hydrogen bond , chemistry , solid state , hydrogen , birch reduction , stereochemistry , medicinal chemistry , organic chemistry , molecule
The title compound, C 6 H 7 CH 2 COOH, is formed by a standard Birch reduction of phenylacetic acid. As expected, a centrosymmetric head‐to‐tail dimer is observed in the solid state, formed through O—H⋯O hydrogen bonds.
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