Gal first isolated patchouli alcohol in 1869, and Montgolfier later formulated its chemical composition (correctly) as C15H26O. Early structural investigation soon established the presence of a saturated tricyclic tertiary alcohol. After several years of careful degradation study,
Büchi and co-workers proposed in 1961 that patchouli alcohol had the structure
1. A subsequent synthesis of material which corresponded to an authentic sample of natural patchouli alcohol appeared to verify Büchi's proposal. File:actual sequence patchouli alcohol.png|center|700px|frameless|Actual sequence for the synthesis of patchouli alcohol. Contains embedded bicyclo[2.2.2]octane motif. However,
Dunitz and co-workers serendipitously discovered in 1963 that Büchi's structure is in fact incorrect. Dunitz
et al. had undertaken
X-ray analysis of the patchouli alcohol diester with
chromic acid, intending to determine the Cr-O-C angles. In the course of their analysis they could not reconcile the X-ray evidence with the "known" structure
1. In a joint paper with Büchi, they collectively proposed that patchouli alcohol in fact had the novel structure
2. The discrepancy had resulted from an unanticipated skeletal rearrangement when patchoulene was treated with
peroxy acid in Büchi's confirmatory synthesis. The rearranged molecule coincidentally exhibited the correct natural product architecture. ==See also==