Aluminium lithium hydride → HCID 22907247, compound
Reaction equation
[H-].[H-].[H-].[H-].[Li+].[Al+3].[N:7]1([CH:16]2[CH2:21][CH2:20][O:19][C:17]2=[O:18])[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[CH:8]1>C1COCC1>[N:7]1([CH:16]([CH2:21][CH2:20][OH:19])[CH2:17][OH:18])[C:15]2[C:10](=[CH:11][CH:12]=[CH:13][CH:14]=2)[CH:9]=[CH:8]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To an ice cooled suspension of LAH (0.84 g, 0.022 mol) in dry THF (60 mL) was added 2-(indol-1-yl)butyrolactone (4 g, 0.02 mol). After 1 hour the mixture was quenched successively with water (0.84 mL), 15% aqueous sodium hydroxide (0.84 mL), and water (2.5 mL). The reaction was filtered and the filtrate was dried, and evaporated. The material obtained, 2.5 g of colorless oil (61% of theory), was used directly in the next reaction.
Workup
- customAfter 1 hour the mixture was quenched successively with water (0.84 mL), 15% aqueous sodium hydroxide (0.84 mL), and water (2.5 mL)
- filtrationThe reaction was filtered
- customthe filtrate was dried
- customevaporated
- customThe material obtained
Sources & evidence
- ORD record
- ord-a7671d011062497b9ef1e95cc9643211
- Source dataset
- uspto-grants-1997_08
- Patent number
- US05661173
Reaction notes
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