An improved protocol for the preparation of 2,6-di(tert-butyl)-4-methylphenyl (BHT) alkanoates

Article abstract of DOI:10.1080/00397919508011385

Treatment of the acid chloride derivatives 2a-e with potassium 2,6-di(tert-butyl)-4-methyl phenoxide 1b afforded the corresponding BHT esters 3a-e in 83-95% yield.

Full text of DOI:10.1080/00397919508011385

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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An Improved Protocol for the
Preparation of 2,6-DI(tert-
Butyl)-4-methylphenyl (BHT)
Alkanoates
P. A. Evans a & A. L. Stanley a
a Lammot du Pont Laboratory, Department of
Chemistry and Biochemistry , University of
Delaware , Newark, DE, 19716
Published online: 23 Sep 2006.
To cite this article: P. A. Evans & A. L. Stanley (1995) An Improved Protocol for
the Preparation of 2,6-DI(tert-Butyl)-4-methylphenyl (BHT) Alkanoates, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 25:4, 515-519, DOI: 10.1080/00397919508011385
To link to this article: http://dx.doi.org/10.1080/00397919508011385
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