反応 #329728

ord-09ded3fd6f6147688b8563e750d9178c

反応方程式

CC(C)(C)OC(=O)N1CCC(=O)C1
1-t-butoxycarbonyl-3-pyrrolidinone
Clc1cc[c]([Mg][Br])cc1
4-chlorophenyl magnesium bromide
CC(C)(C)OC(=O)N1CCC(O)(c2ccc(Cl)cc2)C1
1-t-butoxycarbonyl-3-(4-chlorophenyl)-3-hydroxypyrrolidine
収率 60.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他then quenched by the addition of saturated aqueous NH4OH (8 mL)
  2. 2
    抽出The aqueous layer was extracted with EtOAc (50 mL×2)
  3. 3
    乾燥dried over MgSO4
  4. 4
    濃縮concentrated in vacuo
  5. 5
    その他Chromatographic purification on silica gel (Hexane/EtOAc=3/1)

実験手順

To a stirred solution of 1-t-butoxycarbonyl-3-pyrrolidinone (0.57 g, 3.23 mmol) in THF (10 mL) was added 4-chlorophenyl magnesium bromide (1.0 M, 5.2 mL) under the protection of argon at 0° C. The reaction was stirred at room temperature for 1 hour then quenched by the addition of saturated aqueous NH4OH (8 mL). The aqueous layer was extracted with EtOAc (50 mL×2), dried over MgSO4 and concentrated in vacuo. Chromatographic purification on silica gel (Hexane/EtOAc=3/1) provided 0.57 g 1-t-butoxycarbonyl-3-(4-chlorophenyl)-3-hydroxypyrrolidine (60%). m/z 298 (m+1)

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08653096B2uspto-grants-2014_02