Diisobutylaluminum hydride → 946484-82-8

HRID 1619323Notes

Reaction equation

HRID 1619323 reaction equation
[CH3:1][C:2]1([C:14](OC)=[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]([C:2]1([CH3:1])[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]

Participants

4

Conditions

Temperature
-78 °C

Procedure

To a solution of 1-tert-butyl 2-methyl 2-methylpyrrolidine-1,2-dicarboxylate (3.5 g, 14.3 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 hr 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 (3×50 mL). The combined organics were then washed with brine, dried over Na2SO4, concentrated in vacuo and purified by column chromatography to give 3 g of the desired product.

Workup

  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 (3×50 mL)
  8. washThe combined organics were then washed with brine
  9. dry with materialdried over Na2SO4
  10. concentrationconcentrated in vacuo
  11. custompurified by column chromatography

Sources & evidence

ORD record
ord-8609296e573e472bb6ac5ef70c436f0d
Source dataset
uspto-grants-2014_07
Patent number
US08772301B2

Reaction notes

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