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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515047Generated: October 26, 2026

Hydrogen Peroxide → 2-[(1R,2S)-2-(4-Bromophenyl)cycloprop-1-yl]ethanol

https://huagongshe.com/reaction/515047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant1-Bromo-4-[(1S,2R)-2-vinylcyclopropyl]benzeneHCID 68406252—
SolventTetrahydrofuranHCID 8028—
Product2-[(1R,2S)-2-(4-Bromophenyl)cycloprop-1-yl]ethanolHCID 68407122—

Reaction Steps

To a solution of the alkene from Example 28D (1-bromo-4-[(1S,2R)-2-vinylcyclopropyl]benzene) in anhydrous THF (50 mL) under N2 was added borane-THF at 0° C. The mixture was stirred at room temperature for two hours and then chilled to 0° C. Aqueous hydrogen peroxide (30%) solution was added, the ice bath was removed, and the mixture was allowed to warm to room temperature with continued stirring for 10 minutes. The mixture was quenched with saturated aqueous NH4Cl and extracted with ether. The combined organic extracts were dried (MgSO4) and filtered. The filtrate was concentrated under reduced pressure. The residue was purified on silica gel with 4:1 hexanes/ethyl acetate to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108948B2
Source datasetuspto-grants-2015_08
ORD IDord-b7931fc9c0a14d2a80b26ffe151f938a
Source noteuspto-grants-2015_08