Réaction #1509586

ord-7cdb17f067a04e22aa9305970d553803

Équation de réaction

Cc1[nH]c(=O)ccc1C#N
2-Methyl-6-oxo-1,6-dihydro-pyridine-3-carbonitrile
O=P(Cl)(Cl)Cl
POCl3
Cc1nc(Cl)ccc1C#N
title compound
Cc1nc(Cl)ccc1C#N
6-Chloro-2-methyl-nicotinonitrile

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Températurewas refluxed for 3 h
  2. 2
    AutreThe reaction mixture was dried down in vacuum and ice
  3. 3
    workup.ADDITIONwas added
  4. 4
    ExtractionThe aqueous layer was extracted with EtOAc
  5. 5
    AutreThe organic layer was separated
  6. 6
    Autredried
  7. 7
    Concentrationconcentrated in vacuum

Mode opératoire

A mixture of 2-Methyl-6-oxo-1,6-dihydro-pyridine-3-carbonitrile (44 g) and POCl3 (250 ml) was refluxed for 3 h. The reaction mixture was dried down in vacuum and ice followed by conc. aqueous ammonia (300 ml) was added. The aqueous layer was extracted with EtOAc. The organic layer was separated, dried and concentrated in vacuum affording the title compound (23.5 g, BP (18 mbar) 119-120° C.).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: USRE045323E1uspto-grants-2015_01