Synthesis and reactions of 6-hydroxy-2,4-dimethyl-1,3-benzodioxane

Synthesis and reactions of 6-hydroxy-2,4-dimethyl-1,3-benzodioxane Full article

Journal

Chemistry of Heterocyclic Compounds
ISSN: 0009-3122 , E-ISSN: 1573-8353

Output data

Year: 1983, Volume: 19, Number: 9, Pages: 954-957 Pages count : DOI: 10.1007/BF00506878

Authors

Denisov V. Ya. , Grishchenkova T. N. , Fokin E. P.

Affiliations

1	(Scopus) Kemerovo State University, Kemerovo, 650043, Russian Federation
2	(Scopus) Novosibirsk Institute of Organic Chemistry, Siberian Branch, Academy of Sciences of the USSR, Novosibirsk, 630090, Russian Federation

The reaction of hydroquinone and acetaldehyde in a mixture of acetic and hydrochloric acids (3:1) at 0-5 °C gives 6-hydroxy-2,4-dimethyl-1,3-benzodioxane, which forms ethers and esters at the hydroxy group, undergoes diazo coupling, and, under the influence of acids, undergoes polycondensation with opening of the 1,3-dioxane ring. © 1984 Plenum Publishing Corporation.

Denisov V.Y. , Grishchenkova T.N. , Fokin E.P.
Synthesis and reactions of 6-hydroxy-2,4-dimethyl-1,3-benzodioxane
Chemistry of Heterocyclic Compounds. 1983. V.19. N9. P.954-957. DOI: 10.1007/BF00506878 Scopus РИНЦ OpenAlex

Published print:

Sep 1, 1983

Scopus:	2-s2.0-34250138887
Elibrary:	30861484
OpenAlex:	W2026097359

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