Diisobutylaluminum hydride → 946484-82-8
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
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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
- temperaturewhile maintaining the reaction temperature below −65° C
- customquenched with methanol (10 mL)
- additionThe mixture was then diluted with ethyl acetate (50 mL), saturated NH4Cl
- additionwas added
- stirringthe mixture was stirred vigorously for 20 min at room temperature
- customThe two phases were then separated
- extractionthe aqueous layer was extracted with DCM (3×50 mL)
- washThe combined organics were then washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- 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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