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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 852759Generated: October 26, 2026

Benzyl Bromide → (1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-ol

https://huagongshe.com/reaction/852759

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
Reactant15-Crown-5HCID 36336—
Reactant(1R,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diolHCID 9989289—
Product(1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-olHCID 10036335—

Reaction Conditions

Temperature10 °C

Reaction Steps

To a stirred solution of (1R,2S,4R,5S)-bicyclo[2.2.1]-heptane-2,5-diol (1.15 g, 8.97 mmol) and 15-crown-5 (0.054 mL, 0.269 mmol) in tetrahydrofuran (30.0 mL, 8.97 mmol) were added at 10° C. (ice/water bath) finely ground sodium hydroxide (2.15 g, 53.8 mmol) and 1-(bromomethyl)benzene (1.07 mL, 8.97 mmol). After stirring at 10° C. for 3 h, the mixture was stirred at ambient temperature overnight. The mixture was partitioned between EtOAc and water, and the organic portions were washed with brine, and conc. in vacuo. The crude product was purified by flash column chromatography (0 to 80% of ethyl acetate in hexanes). The title compound was obtained as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07253196B2
Source datasetuspto-grants-2007_08
ORD IDord-85e37eb0157c4996949a0edff5c7ad62
Source noteuspto-grants-2007_08