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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907265Generated: October 31, 2026

Borane → HCID 67043493, compound

https://huagongshe.com/reaction/1907265

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoraneHCID 6331—
ReactantHCID 67043470HCID 67043470—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67043493HCID 67043493102.6%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598160B2
Source datasetuspto-grants-2013_12
ORD IDord-a32f90095f7348abbbf0e25cf2749602
Source noteuspto-grants-2013_12