Sodium Sulfate → HCID 67179158, compound
Reaction equation
[H-].[Al+3].[Li+].[H-].[H-].[H-].C([O:9][C:10](=O)[C@@H:11]([NH2:23])[CH2:12][CH2:13][C:14]([CH3:22])([C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[CH3:15])C.S([O-])([O-])(=O)=O.[Na+].[Na+]>O1CCCC1>[NH2:23][C@@H:11]([CH2:12][CH2:13][C:14]([CH3:22])([C:16]1[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=1)[CH3:15])[CH2:10][OH:9]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a suspension of lithium aluminum hydride (68 mg) in tetrahydrofuran (3 ml) was added a solution of (S)-2-amino-5-methyl-5-phenyl-hexanoic acid ethyl ester (280 mg) in tetrahydrofuran (1 ml) and the mixture was stirred for 3 hours at room temperature. Sodium sulphate solution (1N) was added until gas evolution ceased and the suspension was filtered through Celite. The solvent was evaporated and the residue was purified by chromatography (column: Isolute® Flash-NH2 from Separtis; eluent: dichloromethane/MeOH=90:10) to yield a light yellow oil, (122 mg, 52%); MS (ISP): 208.2 ((M+H)+).
Workup
- filtrationthe suspension was filtered through Celite
- customThe solvent was evaporated
- customthe residue was purified by chromatography (column: Isolute® Flash-NH2 from Separtis; eluent: dichloromethane/MeOH=90:10)
- customto yield a light yellow oil, (122 mg, 52%)
Sources & evidence
- ORD record
- ord-7a4fb07e951642198aec415d94f95b28
- Source dataset
- uspto-grants-2012_08
- Patent number
- US08242153B2
Reaction notes
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