Aluminium lithium hydride → HCID 23039037, compound
Reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].[CH3:7][O:8][C:9]1[CH:17]=[C:16]2[C:12]([CH2:13][CH2:14][CH:15]2[C:18]([N:20]([CH2:29][CH2:30][CH3:31])[CH2:21][CH2:22][C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=O)=[CH:11][CH:10]=1>CCOCC>[CH3:7][O:8][C:9]1[CH:17]=[C:16]2[C:12]([CH2:13][CH2:14][CH:15]2[CH2:18][N:20]([CH2:29][CH2:30][CH3:31])[CH2:21][CH2:22][C:23]2[CH:24]=[CH:25][CH:26]=[CH:27][CH:28]=2)=[CH:11][CH:10]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of 1 g of lithium aluminium hydride in 15 milliliters of anhydrous ether was added a solution of 5 g of the residue of 6-methoxy-N-propyl-N-(2-phenylethyl)-1-indanamide in 15 milliliters of anhydrous ether at a rate which maintained gentle reflux of the reaction mixture. Reflux and stirring were continued for 5 hours. The reaction mixture was then stirred overnight without heating. Destruction of the excess lithium aluminium hydride was completed by cautious dropwise addition of 1 milliliter of water followed by dropwise addition of 1 milliliter of 14% sodium hydroxide solution and subsequent addition of 5 milliliters of water. Stirring was continued for 30 minutes. Filtration yielded a clear ether solution which was dried (MgSO4) and evaporated, yielding 4 grams of an oil, which was used directly in the next step without further purification.
Workup
- temperaturemaintained gentle
- temperaturereflux of the reaction mixture
- temperatureReflux
- stirringThe reaction mixture was then stirred overnight
- temperaturewithout heating
- customDestruction of the excess lithium aluminium hydride
- additionwas completed by cautious dropwise addition of 1 milliliter of water
- additionfollowed by dropwise addition of 1 milliliter of 14% sodium hydroxide solution and subsequent addition of 5 milliliters of water
- stirringStirring
- waitwas continued for 30 minutes
- filtrationFiltration
- customyielded a clear ether solution which
- dry with materialwas dried (MgSO4)
- customevaporated
Sources & evidence
- ORD record
- ord-ffca3e395f0d4436912dfda28c5b4b05
- Source dataset
- uspto-grants-1990_08
- Patent number
- US04946863
Reaction notes
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