Issue 18, 1970

Halogeno-1,4-dioxans and their derivatives. Part V. Bi-1,3-dioxan-2-yl and 2,3,4aα,10aα-tetrahydrobenzo[b]-p-dioxino[2,3-e]-p-dioxin

Abstract

The reaction of trans-2,3-dichloro-1,4-dioxan with trimethylene glycol gives bi-1,3-dioxan-2-yl, and the corresponding reaction with catechol gives 2,3,4aα,10aα-tetrahydrobenzo[b]-p-dioxino[2,3-e]-p-dioxin. The structures of the products are confirmed by n.m.r. spectroscopy, and the chemical shifts and deduced coupling constants are reported. Some mechanisms by which the dichlorodioxan may react are discussed.

Article information

Article type
Paper

J. Chem. Soc. C, 1970, 2457-2459

Halogeno-1,4-dioxans and their derivatives. Part V. Bi-1,3-dioxan-2-yl and 2,3,4aα,10aα-tetrahydrobenzo[b]-p-dioxino[2,3-e]-p-dioxin

R. E. Ardrey and L. A. Cort, J. Chem. Soc. C, 1970, 2457 DOI: 10.1039/J39700002457

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