Acetic Acid → (2R,3S)-N-tert-Butyloxycarbonyl-3-(tert-butyldimethylsilanyloxy)-2-(1-hydroxyethyl)pyrrolidine

HRID 132686ノート

反応式

HRID 132686 の反応式
[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][C@H:10]([O:13][Si:14]([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15])[C@H:9]1[CH:21]=[O:22])=[O:7])([CH3:4])([CH3:3])[CH3:2].C[Mg+].[Br-].[CH3:26]C(O)=O>CCOC(C)=O>[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][C@H:10]([O:13][Si:14]([C:17]([CH3:20])([CH3:19])[CH3:18])([CH3:16])[CH3:15])[C@H:9]1[CH:21]([OH:22])[CH3:26])=[O:7])([CH3:4])([CH3:3])[CH3:2]

参加物

5

反応条件

温度
-78 °C

実験手順

To a solution of 1J (˜0.05 M in THF) at −78° C. was added dropwise MeMgBr (3.0M in Et2O, 3 equiv). The reaction was stirred at −78° C. for 1.5-2 h (quench small aliquot in 10% MeOH/DCM, spot TLC-silica gel, 30% EtOAc/Hex-stain with 5% HCl/MeOH, heat and then ninhydrin, heat). Quench reaction by addition of HOAc (3 equiv) at −78° C. Warm to rt, dilute with EtOAc and wash with a 1:1 mixture of saturated aq. NaHCO3 and brine. Back extract aqueous layer. Combine organic extracts, dry over MgSO4, filter and concentrate. Purification by flash chromatography (silica gel, step gradient 0-10-20% EtOAc in hexane) provided the title compound.

後処理

  1. customquench small aliquot in 10% MeOH/DCM
  2. temperaturespot TLC-silica gel, 30% EtOAc/Hex-stain with 5% HCl/MeOH, heat
  3. temperatureninhydrin, heat)
  4. customQuench
  5. customreaction
  6. temperatureWarm to rt
  7. washwash with a 1:1 mixture of saturated aq. NaHCO3 and brine
  8. extractionBack extract aqueous layer
  9. dry with materialCombine organic extracts, dry over MgSO4
  10. filtrationfilter
  11. concentrationconcentrate
  12. customPurification by flash chromatography (silica gel, step gradient 0-10-20% EtOAc in hexane)

出典と根拠

ORDレコード
ord-fd3d53bcea014a9fb7673c6bdd38efa9
出典データセット
uspto-grants-2008_06
特許番号
US07388027B2

反応ノート

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