Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Reactant | Methyl (βR)-β-[[(1,1-dimethylethoxy)carbonyl]amino]benzenebutanoate | HCID 10447103 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 69235620 | HCID 69235620 | 89% |
Reaction Steps
To a solution (R)-β-[[(1,1-Dimethylethoxy)carbonyl]amino]-benzenebutanoic acid methyl ester (1.5 g, 5.1 mmol, J. Med. Chem. 1985, 28, 434) in THF (10 mL), was added lithium borohydride (218 mg, 10 mmol), followed by ethanol (10 mL), dropwise. After stirring at rt for 18 hours, an additional lithium borohydride (218 mg 10 mmol) was added and stirring continued for 6 hours. The reaction mixture was ice cooled and adjusted to pH 4 by the addition of a 10% citric acid solution. Organic solvents were removed and the resulting cloudy aqueous solution was extracted with dichloromethane. The extracts were combined, dried (MgSO4) and concentrated in vacuo to afford a clear colorless oil residue which was purified by flash chromatography on silica gel eluting with 30% ethyl acetate in hexanes to yield (1.2 g, 89%) of the title compound as a clear colorless oil. MS; (M+H)+=266
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06602883B1 |
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| Source dataset | uspto-grants-2003_08 |
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| ORD ID | ord-8f6100843be8492c9361c8bd8ca5e12c |
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| Source note | uspto-grants-2003_08 |
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