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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1443376Generated: October 30, 2026

Hydrogen Peroxide → Bis(4-bromophenyl)phenylphosphine oxide

https://huagongshe.com/reaction/1443376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantSodium SulfiteHCID 24437—
Reactantbis(4-bromophenyl)phenylphosphineHCID 10364804—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
ProductBis(4-bromophenyl)phenylphosphine oxideHCID 15469924—

Reaction Conditions

Temperature5 °C

Reaction Steps

10.05 g (24 mmol) of bis(4-bromophenyl)phenylphosphine were dissolved in 200 ml of ethyl acetate in a 500 ml four-necked flask with internal thermometer, mechanical stirrer, reflux condenser and dropping funnel and cooled to an internal temperature of 5° C. A solution of 2.25 ml (26.4 mmol) of H2O2 (35%) in 17.5 ml of water was added dropwise over the course of 30 min., and the mixture was stirred at room temperature for a further 12 h. 25 ml of saturated sodium sulfite solution were subsequently added, the organic phase was separated off, washed twice with saturated sodium sulfite solution and dried over sodium sulfate. The solvent was removed under reduced pressure. The purification was carried out firstly by column chromatography on silica using a solvent mixture of initially hexane:ethyl acetate 2:1 to hexane:ethyl acetate 1:1. Further purification was carried out by recrystallisation from heptane/toluene, giving 6.5 g of product in a purity of 99.7% (according to HPLC). 1H-NMR (500 MHz, CDCl3): [ppm] 7.46-7.66 (m). 31P-NMR (CDCl3): [ppm] 28.40.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07659540B2
Source datasetuspto-grants-2010_02
ORD IDord-46db74bf9d4b46f7805560d154a09206
Source noteuspto-grants-2010_02