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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | bis(4-bromophenyl)phenylphosphine | HCID 10364804 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Bis(4-bromophenyl)phenylphosphine oxide | HCID 15469924 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07659540B2 |
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| Source dataset | uspto-grants-2010_02 |
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| ORD ID | ord-46db74bf9d4b46f7805560d154a09206 |
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| Source note | uspto-grants-2010_02 |
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