تفاعل #616569
ord-0a49b87eefda4021a22eb9616a1cb162
معادلة التفاعل
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1تركيزThe mixture was concentrated
- 2workup.ADDITIONthe residue was treated with saturated NaHCO3 solution
- 3استخلاصextracted with DCM (3×)
- 4تجفيفThe extract was dried (Na2SO4)
- 5تركيزconcentrated
- 6أخرىThe residue was dried under vacuum
الإجراء التجريبي
To a solution of (R)-tert-butyl 3-((2,2,2-trifluoro-N-((1R,2S)-2-phenylcyclopropyl)acetamido)methyl)pyrrolidine-1-carboxylate (1.28 g, 3.10 mmol) in dichloromethane (DCM) (12 mL) was added TFA (3 ml, 38.9 mmol), and the mixture was stirred at room temperature for 3 h. The mixture was concentrated and the residue was treated with saturated NaHCO3 solution and extracted with DCM (3×). The extract was dried (Na2SO4) and concentrated. The residue was dried under vacuum to give 950 mg of product as pale yellow oil.