A convenient and simplified preparation of both enantiomers of α- terpinyl chloride

Article abstract of DOI:10.1080/00397910008087247

Several methodologies to produce α-terpinyl chloride from 'hydrochlorination' of limonene were studied and the best results were obtained by reaction with 0.5 mol equiv. SOCl₂ in SiO₂/CH₂Cl₂. Using this methodology (R)- and (S)-α-terpinyl chloride can easily be prepared in good yields from (R)- and (S)-limonene, respectively.

Full text of DOI:10.1080/00397910008087247

Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic
Chemistry
ISSN: 0039-7911 (Print) 1532-2432 (Online) Journal homepage: http://www.tandfonline.com/loi/lsyc20
A Convenient and Simplified Preparation of Both
Enantiomers of α-Terpinyl Chloride
Marcio C. S. de Mattos & Antonio Manzolillo Sanseverino
To cite this article: Marcio C. S. de Mattos & Antonio Manzolillo Sanseverino (2000) A
Convenient and Simplified Preparation of Both Enantiomers of α-Terpinyl Chloride, Synthetic
Communications, 30:11, 1975-1983, DOI: 10.1080/00397910008087247
To link to this article: http://dx.doi.org/10.1080/00397910008087247
Published online: 04 Dec 2007.
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Date: 17 June 2016, At: 14:46