반응 #414473

ord-0c953de4b7d74a7fa5743e83a4ea2e81

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONwas added, under nitrogen
  2. 2
    기타The cooling bath was then removed
  3. 3
    온도The mixture was then cooled again in an ice bath
  4. 4
    workup.ADDITIONtreated with 25 ml of conc. HCl
  5. 5
    여과The mixture was then filtered
  6. 6
    세척the residue washed with methylene chloride
  7. 7
    농축The filtrate was concentrated in vacuo
  8. 8
    기타the 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 4o) 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): & 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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05272156uspto-grants-1993_12