Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane | HCID 6331 | — |
| Reactant | HCID 67043470 | HCID 67043470 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67043493 | HCID 67043493 | 102.6% |
Reaction Steps
5-((S)-1-(4-bromophenyl)ethylamino)-5-oxo-3-phenylpentanoic acid (1.92 g, 4.92 mmol, 1.0 equiv) was dissolved in THF (30 mL) and the resulting solution cooled to 0° C. Borane (1.0 M in THF, 10.5 mL, 10.5 mmol, 2.1 equiv) was added via syringe. After 0.5 h LC-MS showed formation of the alcohol. The excess borane was quenched by the drop-wise addition of 1.0 M aq HCl and the mixture was transferred to a separatory funnel. The layers were separated and the organic layer washed with brine, dried over Na2SO4, filtered and evaporated. The resulting N—((S)-1-(4-bromophenyl)ethyl)-5-hydroxy-3-phenylpentanamide (˜1.9 g, >95% yield) was of sufficient purity to use in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08598160B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-a32f90095f7348abbbf0e25cf2749602 |
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| Source note | uspto-grants-2013_12 |
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