Aluminium lithium hydride → HCID 22499240, compound
Reaction equation
[CH3:1][C:2]1([NH:13][C:14](=O)[C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH2:10][C:9]2[C:4](=[CH:5][C:6]([CH3:12])=[C:7]([CH3:11])[CH:8]=2)[CH2:3]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[CH2:14]([NH:13][C:2]1([CH3:1])[CH2:10][C:9]2[C:4](=[CH:5][C:6]([CH3:12])=[C:7]([CH3:11])[CH:8]=2)[CH2:3]1)[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of N-(2,5,6-trimethyl-indan-2-yl)-benzamide in THF under nitrogen is added LiAlH4 and the mixture refluxed for 48 hours. Quenched at 0° C. with ice/water and extracted with ether, dried (Na2SO4) and solvent removed in vacuo. Purification by chromatography (silica, ethyl acetate/hexane 1:4) gives a colourless oil.
Workup
- temperaturethe mixture refluxed for 48 hours
- customQuenched at 0° C. with ice/water
- extractionextracted with ether
- dry with materialdried (Na2SO4) and solvent
- customremoved in vacuo
- customPurification by chromatography (silica, ethyl acetate/hexane 1:4)
- customgives a colourless oil
Sources & evidence
- ORD record
- ord-460650abdfad4e93952967ec63671c7c
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08658673B2
Reaction notes
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