Diisobutylaluminum hydride → 1-Boc-2-Formylpyrrolidine

HRID 1619394ノート

反応式

HRID 1619394 の反応式
C[C:2]1([C:14]([O-])=[O:15])[CH2:6][CH2:5][CH2:4][N:3]1[C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8].CC(C[AlH]CC(C)C)C>C1(C)C=CC=CC=1>[CH:14]([CH:2]1[CH2:6][CH2:5][CH2:4][N:3]1[C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])=[O:15]

参加物

4

反応条件

温度
-78 °C

実験手順

To a solution of 1-tert-butyl 2-methylpyrrolidine-1,2-dicarboxylate (3.5 g, 15.3 mmol) in toluene at −78° C. was added DIBAL-H (17.6 mL, 30 mmol, 1.7 M) dropwise while maintaining the reaction temperature below −65° C. The reaction was stirred at −78° C. for 2 h and then quenched with methanol (10 mL). The mixture was then diluted with ethyl acetate (50 mL), saturated NH4Cl was added, and the mixture was stirred vigorously for 20 min at room temperature. The two phases were then separated and the aqueous layer was extracted with DCM (2×50 mL). The combined organics were then washed with brine, dried over Na2SO4, concentrated under reduced pressure and purified by column chromatography to give 3 g of the desired product. MS (ESI): 200 (MH+).

後処理

  1. temperaturewhile maintaining the reaction temperature below −65° C
  2. customquenched with methanol (10 mL)
  3. additionThe mixture was then diluted with ethyl acetate (50 mL), saturated NH4Cl
  4. additionwas added
  5. stirringthe mixture was stirred vigorously for 20 min at room temperature
  6. customThe two phases were then separated
  7. extractionthe aqueous layer was extracted with DCM (2×50 mL)
  8. washThe combined organics were then washed with brine
  9. dry with materialdried over Na2SO4
  10. concentrationconcentrated under reduced pressure
  11. custompurified by column chromatography

出典と根拠

ORDレコード
ord-5d574bf8ae7343e7989aa8a4195317cf
出典データセット
uspto-grants-2014_07
特許番号
US08772301B2

反応ノート

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