Diisobutylaluminum hydride → HCID 59564912、化合物

HRID 79493ノート

反応式

HRID 79493 の反応式
[CH3:1]C(C[AlH]CC(C)C)C.[CH3:10][C:11]1([CH3:24])[CH2:15][CH2:14][C:13](=[O:16])[N:12]1[C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18]>CCOCC.CO>[CH3:1][O:16][CH:13]1[N:12]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[C:11]([CH3:24])([CH3:10])[CH2:15][CH2:14]1

参加物

5

反応条件

温度
-78 °C

実験手順

DIBAL-H (73.65 mL, 110.5 mmol, 1.5M in toluene) was added portionwise to a solution of tert-butyl 2,2-dimethyl-5-oxopyrrolidine-1-carboxylate (23.10 g, 108.3 mmol) in dry Et2O (200 mL) cooled to −78° C. The reaction was stirred for 1 hour at −78° C. and then allowed to warm to room temperature and stirred overnight. The reaction was quenched with NH4OH (50 mL) and stirred for 20 minutes. The reaction was then diluted with EtOAc (200 mL), 0.5M Rochelle's Salt (100 mL) was added, and the layers were separated. The organic fraction was washed with 0.5M Rochelle's Salt (2×100 mL), brine (100 mL), dried (MgSO4) and concentrated to an oil. The oil was taken up in a solution of p-TsOH monohydrate (2.06 g, 10.8 mmol) in MeOH (200 mL) and stirred overnight at room temperature. The reaction was then concentrated, taken up in EtOAc (200 mL), washed with saturated Na2CO3 (2×100 mL), brine (50 mL), dried (MgSO4) and concentrated to give tert-butyl 5-methoxy-2,2-dimethylpyrrolidine-1-carboxylate (24.07 g, 96.9% yield) as an oil.

後処理

  1. temperatureto warm to room temperature
  2. stirringstirred overnight
  3. customThe reaction was quenched with NH4OH (50 mL)
  4. stirringstirred for 20 minutes
  5. additionThe reaction was then diluted with EtOAc (200 mL), 0.5M Rochelle's Salt (100 mL)
  6. additionwas added
  7. customthe layers were separated
  8. washThe organic fraction was washed with 0.5M Rochelle's Salt (2×100 mL), brine (100 mL)
  9. dry with materialdried (MgSO4)
  10. concentrationconcentrated to an oil
  11. stirringstirred overnight at room temperature
  12. concentrationThe reaction was then concentrated
  13. washwashed with saturated Na2CO3 (2×100 mL), brine (50 mL)
  14. dry with materialdried (MgSO4)
  15. concentrationconcentrated

出典と根拠

ORDレコード
ord-f1a52b3274944f12be9119560809d5ca
出典データセット
uspto-grants-2014_09
特許番号
US08841304B2

反応ノート

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