Volume 19, Issue 2
Heterocyclic Compounds
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ChemInform Abstract: Structure of 1,5-Benzodioxepines, the Reaction Products of 2-Hydroxy2,3-dihydro-2-phenyl-1,4-benzodioxin and Phenacyl Bromide.

I. B. DZVINCHUK

I. B. DZVINCHUK

Inst. org. khim. AN SSSR, Kiev

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M. O. LOZINSKII

M. O. LOZINSKII

Inst. org. khim. AN SSSR, Kiev

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S. V. SEREDA

S. V. SEREDA

Inst. org. khim. AN SSSR, Kiev

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M. YU. ANTIPIN

M. YU. ANTIPIN

Inst. org. khim. AN SSSR, Kiev

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YU. T. STRUCHKOV

YU. T. STRUCHKOV

Inst. org. khim. AN SSSR, Kiev

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I. E. BOLDESKUL

I. E. BOLDESKUL

Inst. org. khim. AN SSSR, Kiev

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First published: January 12, 1988

Abstract

In the reaction of phenacyl bromide (III) and the benzodioxin (I) which equilibrates with the pyrocatechol ether (II), the benzodioxepine E-(IV) is the only reaction product.

ChemInform Abstract

In the reaction of phenacyl bromide (III) and the benzodioxin (I) which equilibrates with the pyrocatechol ether (II), the benzodioxepine E-(IV) is the only reaction product. Acetylation of E-(IV) gives the acetate E-(VI). (X-ray data of E-(IV): triclinic, space group P1, Z=2; E-(VI): rhombic, space group Pbca, Z=16).

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