Reacción #1687619

ord-52dda751726540faa13449f9467d216d

Ecuación de reacción

N#Cc1cccnc1
3-Cyanopyridine
CI
methyl iodide
CI
methyl iodide
C[n+]1cccc(C#N)c1.[I-]
title compound
Rendimiento 81.0%
C[n+]1cccc(C#N)c1.[I-]
3-Cyano-1-methylpyridinium Iodide
Rendimiento 81.0%

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe mixture was filtered
  2. 2
    Lavadothe solid product was washed with acetone (100 ml)
  3. 3
    OtroAfter drying

Procedimiento

3-Cyanopyridine (1) (104 g, 1 mol) and methyl iodide (150 g, 1.06 mol) in acetone (500 ml) was stirred for 5 hours at room temperature. Then more methyl iodide (20 g, 0.14 mol) was added, and the reaction mixture was stirred overnight at room temperature. The mixture was filtered and the solid product was washed with acetone (100 ml) and then thoroughly with ether. After drying, 199 g (0.81 mol, 81%) of the title compound were obtained, M.P. 145°-150° C.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: USRE036374uspto-grants-1999_11