A convenient synthesis of 2-hydroxybenzenesulfonamide

Article abstract of DOI:10.1080/00397919408012644

Chlorosulfonation of 4-t-butylanisole and formation of the sulfonamide 2, followed by removal of the t-butyl and O-methyl groups with aluminium chloride provides a simple, novel synthesis of 2-hydroxybenzenesulfonamide 3.

Full text of DOI:10.1080/00397919408012644

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Synthetic Communications: An
International Journal for Rapid
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Organic Chemistry
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A Convenient Synthesis of 2-
Hydroxybenzenesulfonamide
Peter F. Drygala a , Andrew F. Kirbya a & Keith G.
Watson b
a ICI Australia Research Group , Ascotvale, Victoria,
3032, Australia
b CSIRO, Division of Chemicals and Polymers , Private
Bag 10, Clayton, Victoria, 3168, Australia
Published online: 23 Sep 2006.
To cite this article: Peter F. Drygala , Andrew F. Kirbya & Keith G. Watson (1994) A
Convenient Synthesis of 2-Hydroxybenzenesulfonamide, Synthetic Communications:
An International Journal for Rapid Communication of Synthetic Organic Chemistry,
24:5, 671-675, DOI: 10.1080/00397919408012644
To link to this article: http://dx.doi.org/10.1080/00397919408012644
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