تفاعل #331430

ord-2b7ec160332042a69b0aac988bc41c04

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    غسيلwashed with an aqueous sodium bicarbonate solution (10%)
  2. 2
    تجفيفThe organic layer was dried with sodium sulfate
  3. 3
    أخرىevaporated under reduced pressure
  4. 4
    أخرىThe crude compound was purified by flash chromatography (Hexanes/EtOAc: 8:2)

الإجراء التجريبي

To a solution of compound 2 (320 mg, 1.17 mmol) in anhydrous dichloromethane (25 mL) was added m-CPBA (316 mg, 1.41 mmol) at 0° C. under an atmosphere of argon. The solution was stirred at 0° C. for 3 h. The solution was then diluted with dichloromethane (50 mL) and washed with an aqueous sodium bicarbonate solution (10%). The organic layer was dried with sodium sulfate and evaporated under reduced pressure. The crude compound was purified by flash chromatography (Hexanes/EtOAc: 8:2) to yield compound 22 (260 mg, 78%). 1H NMR (CDCl3) δ: 0.79 (s, 18-CH3), 0.85 (s, 19-CH3), 0.60-2.11 (residual CH and CH2), 2.43 (dd, J1=18.8 Hz, J2=8.7 Hz, 16β-H), 3.12 (t, J=5.8 Hz, 2×CH of epoxide), 3.16 (broad, s, 2×CH of epoxide).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08653054B2uspto-grants-2014_02