Reaktion #6644
ord-964ba96c58d94d2ea992b45e7a732b3b
Reaktionsgleichung
Edukte
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1workup.ADDITIONwas added, under nitrogen
- 2SonstigeThe cooling bath was then removed
- 3TemperaturThe mixture was then cooled again in an ice bath
- 4workup.ADDITIONtreated with 25 ml of conc. HCl
- 5FiltrationThe mixture was then filtered
- 6Waschenthe residue washed with methylene chloride
- 7EinengenThe filtrate was concentrated in vacuo
- 8Sonstigethe resultant residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes)
Vorschrift
To an ice bath cooled solution of 2 g (10.53 mmol) of 2,2,4,4-tetramethylchroman (Compound 84) in 25 ml of nitromethane was added, under nitrogen, 941 mg (11.99 mmol) of acetyl chloride followed by 1.59 g (11.92) mmol) of aluminum chloride. The cooling bath was then removed and the mixture stirred at room temperature for 16 h. The mixture was then cooled again in an ice bath and treated with 25 ml of conc. HCl. The mixture was then filtered and the residue washed with methylene chloride. The filtrate was concentrated in vacuo and the resultant residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes) to give the title compound as a yellow oil. PMR (CDCl3): δ 1.38 (6H, s), 1.39 (6H, s), 1.87 (2H, s), 2.56 (3H, s), 6.83 (1H, d, J~8.7 Hz), 7.71 (1H, dd, J~8.7 Hz, 2.1 Hz), 7.98 (1H, d, J~2.1 Hz). MS exact mass, m/e 232.1468 (calcd. for C13H20O2, 232.1464).