Abstract
A mixture of 14 g (0.1 mole) of methyl 5-methyl-2-furoate (see p. 23), b.p. 97–99°/12 mm, and 22 ml of 22% aqueous sodium hydroxide solution was prepared in a 100-m1 round-bottomed flask fitted with mercury-sealed stirrer and reflux condenser.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Literature Cited
H. B. Hill and W. L. Jennings, Am. Chem. J. 15, 167 (1893);
I. J. Rinkes, Rec. tray. chim. 49, 1118 (1930);
C. A. 9509 (1931).
K. Maekawa, J. Fac. Agr. Kyushu Univ. 9, 140 (1949);
C. A. 48, 2029g (1954).
J. R. Williard and C. S. Hamilton, J. Am. Chem. Soc. 75, 2370 (1953).
W. R. Kirner and G. H. Richter, J. Am. Chem. Soc. 51, 3131 (1929);
M. M. Runde, E. W. Scott, and J. R. Johnson, J. Am. Chem. Soc. 52, 1284 (1930).
A. L. Mndzhoian and M. G. Grigorian, Doklady Akad. Nauk Arm. SSR (Proc. Acad. Sci. Armenian SSR) 17, 167 (1953).
Editor information
Rights and permissions
Copyright information
© 1959 Springer Science+Business Media New York
About this chapter
Cite this chapter
Mndzhoian, A.L. (1959). 5-Methyl-2-Furoic Acid. In: Mndzhoian, A.L. (eds) Syntheses of Heterocyclic Compounds. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-6658-5_15
Download citation
DOI: https://doi.org/10.1007/978-1-4757-6658-5_15
Publisher Name: Springer, Boston, MA
Print ISBN: 978-1-4757-6660-8
Online ISBN: 978-1-4757-6658-5
eBook Packages: Springer Book Archive