Réaction #1077251
ord-aca09035b44a4c1b965549d2b57f5b1f
Équation de réaction
Réactifs
Aucun
Solvants
Conditions de réaction
Température
80°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1Autrethe resultant reaction mixture
- 2Extractionwas extracted with ether (2×75 mL)
- 3ExtractionThe combined ether extract
- 4Lavagewas washed with water (2×50 mL), 5% Hcl (2×50 mL)
- 5SéchageThe organic layer was dried over magnesium sulfate
- 6Autrethe solvent was removed under reduced pressure
Mode opératoire
To a stirred solution of 2-(3,4-methylenedioxy)phenyl-1-ethanol (1.68 g, 10 mmol) in dry pyridine was added acetic anhydride and the resultant reaction mixture was stirred at 80° C. for 1 h. The reaction mixture was poured into ice-water and was extracted with ether (2×75 mL). The combined ether extract was washed with water (2×50 mL), 5% Hcl (2×50 mL) and then with 5% NaHCO3 (2×50 mL). The organic layer was dried over magnesium sulfate and the solvent was removed under reduced pressure to give 1-acetoxy-2-[(3,4-methylenedioxy)phenyl]ethane as a solid (1.7 g, 81% yield).