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Methyl 5-(Butylthiomethyl)-2-Furoate

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Syntheses of Heterocyclic Compounds
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Abstract

Sodium freed from encrustation (5.75 g, i.e. 0.25 g-atom) was added to 100 ml of dry toluene (Note 1) contained in a 250-ml three-necked round-bottomed flask fitted with stirrer, dropping funnel, and reflux condenser protected by a calcium chloride tube. The mixture was heated until the sodium melted, and the stirrer was then set into motion and the application of heat was stopped; vigorous stirring was continued for 10–15 minutes, during which the temperature of the mixture fell to 40–50°. Gentle stirring of the toluene suspension of finely granulated sodium was continued at this temperature while 30 g (0.33 mole) of freshly distilled 1-butanethiol (Note 2) was added dropwise; the mixture was allowed to stand for several hours.

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Literature Cited

  1. A. L. Mndzhoian and N. M. Divanian, Doklady Akad. Nauk Arm. SSR (Proc. Acad. Sci. Armenian SSR) 17, 164 (1953).

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A. L. Mndzhoian

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© 1959 Springer Science+Business Media New York

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Mndzhoian, A.L. (1959). Methyl 5-(Butylthiomethyl)-2-Furoate. In: Mndzhoian, A.L. (eds) Syntheses of Heterocyclic Compounds. Springer, Boston, MA. https://doi.org/10.1007/978-1-4757-6658-5_8

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  • DOI: https://doi.org/10.1007/978-1-4757-6658-5_8

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4757-6660-8

  • Online ISBN: 978-1-4757-6658-5

  • eBook Packages: Springer Book Archive

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