Reaktion #1687619

ord-52dda751726540faa13449f9467d216d

Reaktionsgleichung

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

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe mixture was filtered
  2. 2
    Waschenthe solid product was washed with acetone (100 ml)
  3. 3
    SonstigeAfter drying

Vorschrift

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.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE036374uspto-grants-1999_11