Abstract
The condensation of 1-hydroxy-2-aminonapnthalene with furoyl chloride in 1-methyl-2-pyrrolidone medium afforded 2-(fur-2-yl)naphtho[2,1-d]oxazole. It was involved in reactions of electrophylic substitution like nitration, bromination, sulfonation, formylation, and acylation. In all cases the substituent enters in position 2 of the furan ring.
Similar content being viewed by others
References
Pechkin, A.A. and El’chaninov, M.M., Izv. Vys. Ucheb. Zaved. Sev-Kav. Region, Estestv. Nauki, 2000, no. 4. p. 48.
Pozharskiy, F.T. and Oleinikova, L.Ya, Khim. Geterotsikl. Soed., 1972, no. 11, p. 1555.
El’chaninov, M.M., Oleinikova, L.Ya., and Simonov, A.M., Khim. Geterotsikl. Soed., 1979, no. 8, p. 1047.
Dorofeenko, G.N., Zh. Obshch. Khim., 1961, vol. 31, no. 5, p. 994.
Pozharskii, A.F., Teoreticheskie osnovy khimii geterotsiklov (Theoretical Basis of Chemistry of Heterocyclic Compounds), Moscow: Khimiya, 1985.
Terent’ev, A.P. and Kazitsina, L.A., Zh. Org. Khim., 1948, vol. 18, no. 4, p. 723.
Dunn, G.L., Actor, P., and DiPasquo, V.J., Med. Chem., 1966, no. 9, p. 751.
Author information
Authors and Affiliations
Corresponding author
Additional information
Original Russian Text © E.V. Illenzeer, A.A. Aleksandrov, M.M. El’chaninov, 2013, published in Zhurnal Obshchei Khimii, 2013, Vol. 83, No. 1, pp. 103–106.
Rights and permissions
About this article
Cite this article
Illenzeer, E.V., Aleksandrov, A.A. & El’chaninov, M.M. 2-(Fur-2-yl)naphtho[2,1-d]oxazole. Synthesis and some transformations. Russ J Gen Chem 83, 95–98 (2013). https://doi.org/10.1134/S1070363213010167
Received:
Published:
Issue Date:
DOI: https://doi.org/10.1134/S1070363213010167