Aluminium lithium hydride → HCID 86756069, compound
Reaction equation
[CH2:1]([N:8]1[CH2:12][C@:11]2([CH2:19][C:20](O)=[O:21])[C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[C@@H:10]2[CH2:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[H-].[Al+3].[Li+].[H-].[H-].[H-]>O1CCCC1>[CH2:1]([N:8]1[CH2:12][C@:11]2([CH2:19][CH2:20][OH:21])[C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=3[C@@H:10]2[CH2:9]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3.32 g of the product obtained in Step C are introduced, in portions, into a suspension composed of 0.73 g of lithium aluminium hydride and 53 ml of tetrahydrofuran. After 2 hours at ambient temperature, the medium is hydrolysed in the cold state and the precipitate formed is filtered off. After evaporating off the solvent, the expected product is isolated.
Workup
- customthe precipitate formed
- filtrationis filtered off
- customAfter evaporating off the solvent
Sources & evidence
- ORD record
- ord-815f1672dee14c5dad411a051ac53e2c
- Source dataset
- uspto-grants-2000_11
- Patent number
- US06153640
Reaction notes
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