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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370167Generated: October 30, 2026

6-Oxabicyclo[3.1.0]hexane → (1S,2R)-2-(3,5-difluorophenyl)cyclopentanol

https://huagongshe.com/reaction/2370167

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Oxabicyclo[3.1.0]hexaneHCID 9244—
ReactantHCID 178505930HCID 178505930—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTetrahydrofuranHCID 8028—
Product(1S,2R)-2-(3,5-difluorophenyl)cyclopentanolHCID 1097644390%

Reaction Steps

A flask was charged with (3,5-difluorophenyl)magnesium bromide (149 mL, 149 mmol) and copper (I) iodide (1.901 g, 9.98 mmol). To this reaction mixture, 6-oxabicyclo[3.1.0]hexane (12.53 g, 149 mmol) dissolved in THF (25 mL) was added dropwise. The reaction mixture warmed upon the addition of the epoxide. The reaction was stirred at rt for 2 h at rt. The reaction mixture was quenched by the addition of a solution of ammonium chloride. Ether was added and the organic layer was collected, dried (Na2SO4) and concentrated. The crude product was purified by column chromatography on silica gel to afford (1S,2R)-2-(3,5-difluorophenyl)cyclopentanol (26.5 g, 134 mmol, 90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710061B2
Source datasetuspto-grants-2014_04
ORD IDord-738021ff7e6b4ec09688a076b86e5068
Source noteuspto-grants-2014_04