تفاعل #81088

ord-5cebe00fda724fdeb97e45b2b4d2ba77

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحthen filtered
  2. 2
    تركيزThe filtrate was concentrated in vacuo
  3. 3
    workup.ADDITIONThe residue was diluted in ethyl acetate (100 ml)
  4. 4
    غسيلwashed with a 10% aqueous solution of potassium bisulfate (50 ml) and brine
  5. 5
    تجفيفdried (sodium sulfate)
  6. 6
    تركيزconcentrated in vacuo
  7. 7
    أخرىThe crude product (4.61 g) was purified by flash chromatography (60 g-Merck silica gel, 1:45:54 acetic acid/ethyl acetate/hexane)

الإجراء التجريبي

To a light green solution of potassium thioacetate (3.94 g, 34.5 mmol) in acetonitrile (150 ml) was added a solution of (R)-2-bromopropanoic acid (4.8 g, 31 mmol) in acetonitrile (12 ml) at room temperature under an argon atomosphere. The resulting white slurry was stirred at room temperature for 2 hours then filtered. The filtrate was concentrated in vacuo. The residue was diluted in ethyl acetate (100 ml), washed with a 10% aqueous solution of potassium bisulfate (50 ml) and brine, dried (sodium sulfate), and concentrated in vacuo. The crude product (4.61 g) was purified by flash chromatography (60 g-Merck silica gel, 1:45:54 acetic acid/ethyl acetate/hexane) to afford 3.7 g of the title product as a light yellow oil; [α]D =-114° (c=0.50, methanol).

المصدر

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