Hydrochloric Acid → HCID 22618845, compound
Reaction equation
[BH4-].[Li+].[CH2:3]([C:5]([NH:27][C:28](OC)=[O:29])([CH2:11][CH2:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)=[CH:15][CH:14]=1)[C:6]([O:8]CC)=O)[CH3:4].Cl.C(OCC)(=O)C>O1CCCC1>[CH2:3]([C:5]1([CH2:11][CH2:12][C:13]2[CH:14]=[CH:15][C:16]([O:19][CH2:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)=[CH:17][CH:18]=2)[CH2:6][O:8][C:28](=[O:29])[NH:27]1)[CH3:4]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
Lithium borohydride (3.2 g) was added to a solution of ethyl 2-ethyl-2-methoxycarbonylamino-4-(4-benzyloxyphenyl)butanoate (29 g) in tetrahydrofuran (370 ml) and the mixture was refluxed under heating for 5 hours. 2 M Hydrochloric acid (40 ml) was added to the reaction mixture and the mixture was stirred for 2.5 hours. Ethyl acetate was added to the reaction mixture, the mixture was washed with water and a saturated brine and dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure. Treatment of the residue with hexane and ethyl acetate gave the subject compound (11 g). Then, the mother liquid was concentrated under reduced pressure and the obtained residue was purified by silica gel column chromatography (eluent; ethyl acetate:n-hexane=1:2) to give the subject compound (11 g).
Workup
- temperaturethe mixture was refluxed
- temperatureunder heating for 5 hours
- washthe mixture was washed with water
- dry with materiala saturated brine and dried over anhydrous sodium sulfate
- distillationThe solvent was distilled away under reduced pressure
Sources & evidence
- ORD record
- ord-83c55dd263d34624a76f2c2fac7f1cae
- Source dataset
- uspto-grants-2002_04
- Patent number
- US06372800B1
Reaction notes
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