Réaction #5136
ord-f1b3d2d807af4226b0d71e242805c55b
Équation de réaction
methyl 11-chloroacetamido-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate
imidazole
→
product
Methyl 11-(1-imidazolyl)acetamido-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate
Réactifs
Aucun
Solvants
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Températureto cool
- 2workup.DISTILLATIONthe solvent was distilled off under reduced pressure
- 3ExtractionThe obtained residue was extracted with 300 ml of methylene chloride
- 4LavageThe extract was washed successively with saturated sodium bicarbonate aqueous solution and saturated sodium chloride aqueous solution
- 5SéchageAfter drying over anhydrous sodium sulfate
- 6workup.DISTILLATIONthe solvent was distilled off under reduced pressure
- 7LavageThe resulting residue was subjected to silica gel column chromatography (eluting solvent; chlororform:methanol=10:1)
Mode opératoire
Crude methyl 11-chloroacetamido-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate, 3.0 g, was heated to reflux for 4 hours in 100 ml of toluene together with 0.9 g of imidazole. After allowing to cool, the solvent was distilled off under reduced pressure. The obtained residue was extracted with 300 ml of methylene chloride. The extract was washed successively with saturated sodium bicarbonate aqueous solution and saturated sodium chloride aqueous solution. After drying over anhydrous sodium sulfate, the solvent was distilled off under reduced pressure. The resulting residue was subjected to silica gel column chromatography (eluting solvent; chlororform:methanol=10:1) to give 1.6 g of the product.