Reacción #1687632
ord-5014743c50fb477e92146cc0f89facb6
Ecuación de reacción
charcoal
acetone oxime
nicotinoyl chloride
ether
→
82
4-Methyl-2-(3-pyridyl)-oxazole
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Temperatura
120°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1workup.ADDITIONwas added dropwise under a nitrogen atmosphere
- 2OtroA violent reaction
- 3TemperaturaAfter cooling the mixture
- 4Filtraciónfiltered
- 5Otrothe ether phase separated
- 6ExtracciónThe aqueous phase was extracted with 2×200 ml of ether
- 7Secadothe combined organic phase dried over magnesium sulphate
- 8OtroRemoval 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%).