Reacción #944007

ord-179d2732f0504702aa2c056904bc89d8

Ecuación de reacción

CSc1ccc(C=Nc2ccc(F)cc2)cc1
aniline
CSc1ccc(C=Nc2ccc(F)cc2)cc1
4-fluoro-N-(4-methylthiobenzylidene)aniline
C[Si](C)(C)C#N
trimethylsilyl cyanide
CSc1ccc(C(C#N)Nc2ccc(F)cc2)cc1
title compound
CSc1ccc(C(C#N)Nc2ccc(F)cc2)cc1
α-(4-Fluoroanilino)-α-(4-methylthiophenyl) acetonitrile

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Procedimiento

Following a procedure similar to that described in Example 1(i), but using 4-methylthiobenzaldehyde and 4-fluoroaniline as starting materials, 4-fluoro-N-(4-methylthiobenzylidene)aniline was obtained in a yield of 89%. This aniline compound and trimethylsilyl cyanide were then reacted together in a similar manner to that described in Example 1(ii), to give the title compound as a slightly yellow powder (yield 47%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE039420E1uspto-grants-2006_12