Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46102Generated: October 25, 2026

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

https://huagongshe.com/reaction/46102

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 numberUS08541592B2
Source datasetuspto-grants-2013_09
ORD IDord-0398e47c3d9a4f728465e8b40c186dab
Source noteuspto-grants-2013_09