Reacción #1687632

ord-5014743c50fb477e92146cc0f89facb6

Ecuación de reacción

C
charcoal
CC(C)=NO
acetone oxime
O=C(Cl)c1cccnc1
nicotinoyl chloride
CCOCC
ether
Cc1coc(-c2cccnc2)n1
82
Cc1coc(-c2cccnc2)n1
4-Methyl-2-(3-pyridyl)-oxazole

Condiciones de reacción

Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.ADDITIONwas added dropwise under a nitrogen atmosphere
  2. 2
    OtroA violent reaction
  3. 3
    TemperaturaAfter cooling the mixture
  4. 4
    Filtraciónfiltered
  5. 5
    Otrothe ether phase separated
  6. 6
    ExtracciónThe aqueous phase was extracted with 2×200 ml of ether
  7. 7
    Secadothe combined organic phase dried over magnesium sulphate
  8. 8
    OtroRemoval of solvent in vacuo

Procedimiento

To 10 g (0.140 mol) of acetone oxime cooled to -10° C. neat nicotinoyl chloride (40 g, 0.280 mol) was added dropwise under a nitrogen atmosphere. A violent reaction occured and the mixture became quickly solid. The solid was heated to 120° C. for 3 h. After cooling the mixture was dissolved in ice water and ammonia. After addition of 300 ml of ether the mixture was treated with charcoal, filtered, and the ether phase separated. The aqueous phase was extracted with 2×200 ml of ether, and the combined organic phase dried over magnesium sulphate. Removal of solvent in vacuo gave crude 82 as a red oil. Yield: 3.9 g (0.024 mol, 17%).

Fuente

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