تفاعل #81087

ord-2b57d1dc57fe46baba24008f1f75b5d9

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

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

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05616775uspto-grants-1997_04