반응 #81087

ord-2b57d1dc57fe46baba24008f1f75b5d9

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과The slurry was filtered
  2. 2
    농축The filtrate was concentrated in vacuo
  3. 3
    workup.ADDITIONThe residue was diluted in ether (50 ml)
  4. 4
    세척washed with two portions of 5% aqueous sodium thiosulfate (50 ml) and brine (25 ml)
  5. 5
    건조dried (magnesium sulfate)
  6. 6
    농축concentrated in vacuo
  7. 7
    기타The pale yellow oil was purified by flash chromatography (Merck silica gel, 12×3 cm., 10% methanol/methylene chloride)

실험 절차

A slurry of potassium thioacetate (750 mg, 6.58 mmol) and acetonitrile (10 ml, molecular sieves dried) was cooled to 0° C. and treated with a solution of (R)-2-bromo-4,4-dimethylpentanoic acid from part (a) in acetonitrile (2 ml) over 5 minutes. The reaction mixture was allowed to warm to room temperature and stirred for 2.5 hours. The slurry was filtered. The filtrate was concentrated in vacuo. The residue was diluted in ether (50 ml), washed with two portions of 5% aqueous sodium thiosulfate (50 ml) and brine (25 ml), dried (magnesium sulfate), and concentrated in vacuo. The pale yellow oil was purified by flash chromatography (Merck silica gel, 12×3 cm., 10% methanol/methylene chloride) affording 575 mg of title product as a pale yellow oil.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05616775uspto-grants-1997_04