Beilstein Journal of Organic Chemistry (Jul 2011)

Scalable synthesis of (1-cyclopropyl)cyclopropylamine hydrochloride

  • Sergei I. Kozhushkov,
  • Alexander F. Khlebnikov,
  • Rafael R. Kostikov,
  • Dmitrii S. Yufit,
  • Armin de Meijere

DOI
https://doi.org/10.3762/bjoc.7.113
Journal volume & issue
Vol. 7, no. 1
pp. 1003 – 1006

Abstract

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1-Cyclopropylcyclopropanecarboxylic acid (2), which is accessible on a large scale (900 mmol) from 1-bromo-1-cyclopropylcyclopropane (1) in 64% yield (89% on a 12.4 mmol scale), has been subjected to a Curtius degradation employing the Weinstock protocol to furnish the N-Boc-protected (1-cyclopropyl)cyclopropylamine 3 (76%). Deprotection of 3 with hydrogen chloride in diethyl ether gave the (1-cyclopropyl)cyclopropylamine hydrochloride (4·HCl) in 87% yield.

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