Action of peracetic acid on (+)-sabinol
Journal of the Chemical Society C: Organic Pub Date: DOI: 10.1039/J39690000716
Abstract
The compound said to have the constitution C10H18O3, obtained by Henderson and Robertson from the action of peracetic acid on (+)-sabinol, has been shown to be p-menthane-1α,2β,4β-triol (C10H20O3) by its synthesis from (+)-terpinen-4-ol. The origin of the triol from the sabinol reaction is discussed and it is suggested that it actually arises from terpinen-4-ol, present either as impurity or as a product of the reaction of acetic acid on sabinol. The products of this reaction have been investigated and terpinen-4-ol has been found to be present. (+)-2-endo-Hydroxy-1,4-cineole was obtained by acid-catalysed rearrangement of (+)-terpinen-4-ol α-epoxide.
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Journal Name:Journal of the Chemical Society C: Organic
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CAS no.: 89640-58-4