Journal of the American Chemical Society

The identity of Heilpern's “pinacolylthiourea” and the preparation of authentic 2-thiono-4, 4, 5, 5-tetramethylimidazolidine

R Sayre

Index: Sayre Journal of the American Chemical Society, 1955 , vol. 77, p. 6689

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Citation Number: 70

Abstract

The reaction of aqueous ammonia with a mixture of acetone and carbon disulfide was investigated by Heilpern, who isolated the principal product (his so-called “pinacolylthiourea”) as crystals which melted with decomposition at 240-243 O. As possible structures for the presumed new compound, to which he erroneously assigned the empirical formula C, H14NzS, he considered the saturated cyclic thioureas I and 11, deciding in ...