Réaction #531786
ord-b02e27fc945948d4979a75e5b131dc9b
Équation de réaction
water
4-aminobenzyl cyanide
pyridine
chloride
→
desired product
N-(4-cyanomethylphenyl) p-menthanecarboxamide
Réactifs
Aucun
Conditions de réaction
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1AutreThe mixture was separated
- 2LavageThe organic layer was washed with 50 mL of water and 50 mL of brine
- 3SéchageThe organic layer was dried over MgSO4
- 4AutreThe solvent was evaporated in vacuo
- 5Autreto afford the crude product, which
- 6Autrewas recrystallized from hexanes
Mode opératoire
To a flask, were added 6.6 g (50 mmol) of 4-aminobenzyl cyanide, 4.04 mL of pyridine and 100 mL MtBE. To this mixture, 10 g of p-menthane-3-carbon*yl chloride were added dropwise over 5 minutes. The reaction mixture was stirred for 24 h. To the reaction mixture, 50 mL of water were added. The mixture was separated. The organic layer was washed with 50 mL of water and 50 mL of brine. The organic layer was dried over MgSO4. The solvent was evaporated in vacuo to afford the crude product, which was recrystallized from hexanes to afford 10.1 g of the desired product with the following spectroscopic properties: