反応 #89699

ord-7420de5697854d5086f76dcd2b4cd9fd

反応方程式

[Cl-].[NH4+]
NH4Cl
CC(C)(C)OC(=O)N1CCC(=O)C1
tert-butyl 3-oxopyrrolidine-1-carboxylate
[Br][Mg][c]1ccccc1
phenylmagnesium bromide
CC(C)(C)OC(=O)N1CCC(O)(c2ccccc2)C1
desired product
収率 49.2%
CC(C)(C)OC(=O)N1CCC(O)(c2ccccc2)C1
tert-butyl 3-hydroxy-3-phenylpyrrolidine-1-carboxylate
収率 49.2%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The reaction was heated
  2. 2
    温度to reflux for 15 min
  3. 3
    抽出extracted with ether (3×)
  4. 4
    乾燥The combined organic layers were dried over Na2SO4
  5. 5
    濃縮concentrated in vacuo
  6. 6
    その他The crude residue was purified by flash column chromatography

実験手順

To a solution of tert-butyl 3-oxopyrrolidine-1-carboxylate (1 g, 5.40 mmol) in ether (20 ml) was added dropwise phenylmagnesium bromide (10.3 mL, 3.0 M in ether, 6.21 mmol) at rt under nitrogen. The reaction was heated to reflux for 15 min, then cooled to rt, poured into sat. NH4Cl, extracted with ether (3×). The combined organic layers were dried over Na2SO4, concentrated in vacuo. The crude residue was purified by flash column chromatography to yield the desired product (700 mg, 49.24%). LCMS (M+H) 264.160.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09440958B2uspto-grants-2016_09