Patchoulol or patchouli alcohol (C15H26O) is a sesquiterpene alcohol found in patchouli.[1] Patchouli oil is an important material in perfumery. The (−)-optical isomer is one of the organic compounds responsible for the typical patchouli scent. Patchoulol is obtained by fermentation of leaves of Pogostemon cablin.[2]
Patchoulol is also used in the synthesis of the chemotherapy drug Taxol.[citation needed]
Structure determination
Gal first isolated patchouli alcohol in 1869, and Montgolfier later formulated its chemical composition (correctly) as C15H26O.[3] Early structural investigation soon established the presence of a saturated tricyclic tertiary alcohol.[4] After several years of careful degradation study, Büchi and co-workers proposed 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.[5]
Proposed sequence for the synthesis of patchouli alcohol.Actual sequence for the synthesis of patchouli alcohol. Contains embedded bicyclo[2.2.2]octane motif.
However, Dunitz and co-workers serendipitously discovered 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.[6] 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.[7]
^Deguerry, F.; Pastore, L.; Wu, S.; Clark, A.; Chappell, J.; Schalk, M. (2006). "The diverse sesquiterpene profile of patchouli, Pogostemon cablin, is correlated with a limited number of sesquiterpene synthases". Archives of Biochemistry and Biophysics. 454 (2): 123–136. doi:10.1016/j.abb.2006.08.006. PMID16970904.
^Büchi, G.; Erickson, R. E.; Wakabyashi, N. (1961). "Terpenes. XVI. Constitution of Patchouli Alcohol and Absolute Configuration of Cedrene". Journal of the American Chemical Society. 83 (4): 927–938. doi:10.1021/ja01465a042.
^Simonsen, J.; Barton, D. H. R. (1952). The Terpenes. Vol. 111. Cambridge University Press, London.
^Büchi, G.; Macleod, W. D. (1962). "Synthesis of Patchouli Alcohol". Journal of the American Chemical Society. 84 (16): 3205–3206. doi:10.1021/ja00875a047.
^Dobler, M.; Dunitz, J. D.; Gubler, B.; Weber, H. P.; Büchi, G. & Padilla, O. J. (1963). "The Structure of Patchouli Alcohol". Proc. Chem. Soc. December: 383. doi:10.1039/PS9630000357.
^Nicolaou, K. C.; Snyder, S. A. (2005). "Chasing Molecules That Were Never There: Misassigned Natural Products and the Role of Chemical Synthesis in Modern Structure Elucidation". Angewandte Chemie International Edition. 44 (7): 1012–1044. doi:10.1002/anie.200460864. PMID15688428.
![Actual sequence for the synthesis of patchouli alcohol. Contains embedded bicyclo[2.2.2]octane motif.](File:Actual_sequence_patchouli_alcohol.png)
