Abstract
3-Bromofuran has been obtained in good yield by the reaction of 4, 5-dibromo-3, 6-endoxohexahydrophthalic anhydride with quinoline at 210–220° C. It has been shown that the reaction of 3-bromofuran with acetic anhydride in the presence of perchloric acid forms 2-acetyl-3-bromofuran.
Similar content being viewed by others
References
Ya. L. Gol'dfarb and L. D. Tarasova, DAN,163, 1393, 1965.
H. Gilman and G. F. Wright, J. Am. Chem. Soc.,55, 3302, 1933.
W. Levis, US patent no. 2773882, 1956; RZhKh, 12760p, 1959.
S. Gronowitz and G. Sorlin, Acta Chem. Scand.,15, 1419, 1961; RZhKh, 11Zh222, 1962.
Z. N. Nazarova, Yu. A. Babaev, and T. N. Natalina, ZhOKh,33, 1431, 1963.
Z. N. Nazarova, Yu. A. Babaev, and V. A. Anisimova, USSR patent no. 157451, 1963; Byull. izobr., no. 18, 1963.
I. P. Tsukervanik, N. K. Rozhkova, and I. B. Romanova, DAN UzbekSSR,9, 113, 1954.
A. P. Dunlop and F. N. Peters, The Furans, New York, 160, 1953.
L. M. Nazarova and Ya. K. Syrkin, ZhOKh,14, 777, 1949.
Dictionary of Organic Compounds, Vol. 1 [Russian translation], IL, Moscow, p. 296, 1949.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Nazarova, Z.N., Babaev, Y.A. & Umanskaya, L.G. Synthesis and reactions ofβ-substituted furans. Chem Heterocycl Compd 5, 12 (1969). https://doi.org/10.1007/BF01031750
Issue Date:
DOI: https://doi.org/10.1007/BF01031750