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1-[1-[2-(2,4-Dinitrophenyl)hydrazono]ethyl]cyclopropane synthesis

1synthesis methods
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Yield:790-13-6 59%

Reaction Conditions:

with acetic acid in ethanol; for 10 h;Reflux;

Steps:

Synthesis of 4-nitro- and 2,4-dinitrophenylhydrazones

General procedure: A mixture of arylhydrazine (5mmol), ketone (6 mmol) and AcOH (0.5 mL) in EtOH (20 mL) was heated to refluxfor the time indicated below. The product was purified by recrystallizationfrom ethanol.

References:

Salikov, Rinat F.;Belyy, Aleksandr Yu.;Tomilov, Yury V. [Tetrahedron Letters,2014,vol. 55,# 43,p. 5936 - 5939] Location in patent:supporting information