반응 #168341
ord-6a5df74267484998a9689d2c3c05eb2b
반응 방정식
반응 조건
후처리
- 1기타quenched with saturated NaHCO3 solution
- 2기타The layers were separated
- 3추출the aqueous layer was extracted with dichloromethane (3×10 mL)
- 4세척The combined organic layers were washed with brine
- 5건조dried over anhydrous Na2SO4
- 6여과filtered
- 7농축concentrated in vacuo
- 8기타Purification of the residue on a silica gel column (0 to 50% EtOAc/hexanes)
실험 절차
Triethylamine (0.43 mL, 3.4 mmol) was added to a −40° C. solution of (2R,3R)-3-(benzylamino)pentan-2-ol (220 mg, 1.1 mmol) in dichloromethane (100 mL), followed by the addition of 2-chloroacetyl chloride (0.10 mL, 1.1 mmol) dropwise. The reaction mixture was stirred at −40° C. for 1 hour and then quenched with saturated NaHCO3 solution. The layers were separated, and the aqueous layer was extracted with dichloromethane (3×10 mL). The combined organic layers were washed with brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. Purification of the residue on a silica gel column (0 to 50% EtOAc/hexanes) afforded N-benzyl-2-chloro-N-((2R,3R)-2-hydroxypentan-3-yl)acetamide. MS APCl calc'd for C14H20ClNO2 [M+H]+ 270. found 270.