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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45460Generated: October 30, 2026

Potassium Bromide → (2-(Benzyloxy)biphenyl-3-yl)(phenyl)methanone

https://huagongshe.com/reaction/45460

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium BromideHCID 253877—
ReactantSodium BicarbonateHCID 516892—
ReactantSodium HypochloriteHCID 23665760—
Reactant(2-(Benzyloxy)biphenyl-3-yl)(phenyl)methanolHCID 58238513—
CatalystTempoHCID 2724126—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(2-(Benzyloxy)biphenyl-3-yl)(phenyl)methanoneHCID 5823852388.4%

Reaction Steps

A solution of crude 24 (50 mmol) in dichloromethane (200 mL) and a solution of potassium bromide (0.7 g) in water (10 mL) were mixed together and stirred in an ice bath. TEMPO (120 mg) was added and a solution of 37% aqueous sodium hypochlorite (48 mL), sodium bicarbonate (5 g) and water (to 100 mL) was added in portions at such a rate that the temperature did not exceed 5° C. Stirring was continued on the ice bath for 20 min. The reaction mixture was diluted with dichloromethane (200 mL) and washed with water (300 mL), 1N hydrochloric acid (300 mL), water (300 mL) and brine (300 mL). The organic layer was dried over sodium sulfate, filtered and the solvent was removed on a rotary evaporator. The crude product (19 g) was purified by chromatography on silica (350 g) with 2% ethyl acetate in heptane (7 L). Pure 25 (16.1 g, 88%) was isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541522B2
Source datasetuspto-grants-2013_09
ORD IDord-ca5c1650bd1d4738b4ba3bf245bbc7a2
Source noteuspto-grants-2013_09