Organic & biomolecular chemistry

Aluminium triflate: a remarkable Lewis acid catalyst for the ring opening of epoxides by alcohols

DBG Williams, M Lawton

Index: Bradley; Williams; Lawton, Michelle Organic and Biomolecular Chemistry, 2005 , vol. 3, # 18 p. 3269 - 3272

Full Text: HTML

Citation Number: 77

Abstract

Initially, we conducted our experiments using styrene oxide. Using the protocol set out by Green in a 1987 patent, 6 six equivalents of methanol or ethanol (with no added solvent) and 0.1% of Al(OTf) 3 were added to styrene oxide and the mixture was heated under reflux for one hour. The reaction afforded excellent yields of the glycol ether where the nucleophile had attacked at the more hindered carbon atom of the epoxide ring (Scheme 1).

Related Articles:

Hydroboration. 57. Hydroboration with 9-borabicyclo [3.3. 1] nonane of alkenes containing representative functional groups

[Brown, Herbert C.; Chen, Jackson C. Journal of Organic Chemistry, 1981 , vol. 46, # 20 p. 3978 - 3988]

More Articles...