A formal, one-pot β-chlorination of primary alcohols and its utilization in the transformation of terpene feedstock and the synthesis of a C2-symmetrical terminal bis-epoxide

J Org Chem. 2014 Feb 7;79(3):976-83. doi: 10.1021/jo402422b. Epub 2014 Jan 28.

Abstract

A one-pot transformation of alkan-1-ols into 2-chloroalkan-1-ols is described. As a practical application, terpene-derived primary alcohols were converted into semiochemicals such as olfactory lactones (aerangis lactone, whisky lactone, and cognac lactone) and pheromones (cruentol and ferrugineol). Using heptane-1,7-diol as a bifunctional substrate, the corresponding bis-epoxide was synthesized by bidirectional synthesis in good yield and high enantioselectivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alcohols / chemistry*
  • Epoxy Compounds / chemical synthesis*
  • Epoxy Compounds / chemistry
  • Halogenation
  • Molecular Structure
  • Stereoisomerism
  • Terpenes / chemistry*

Substances

  • Alcohols
  • Epoxy Compounds
  • Terpenes