반응 #6644
ord-964ba96c58d94d2ea992b45e7a732b3b
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후처리
- 1workup.ADDITIONwas added, under nitrogen
- 2기타The cooling bath was then removed
- 3온도The mixture was then cooled again in an ice bath
- 4workup.ADDITIONtreated with 25 ml of conc. HCl
- 5여과The mixture was then filtered
- 6세척the residue washed with methylene chloride
- 7농축The filtrate was concentrated in vacuo
- 8기타the resultant residue was purified by flash chromatography (silica; 10% ethyl acetate in hexanes)
실험 절차
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).