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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075419Generated: October 30, 2026

Triphenylphosphine → Triphenylphosphine Oxide

https://huagongshe.com/reaction/1075419

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantPhosphineHCID 24404—
ReactantBROMINE CHLORIDE (BrCl)HCID 61697—
ReactantHCID 22134543HCID 22134543—
ProductTriphenylphosphine OxideHCID 1309795%

Reaction Steps

A solution of triphenylphosphine (2.62 g, 10 mmol) in a methanol-EDC mixture (100 mL, 50:50, Vol.) was placed in a 250-mL round bottom flask and cooled in an ice bath. Stabilized BrCl (15 wt. % solution, 7.5 mL, 12 mmol) was added dropwise to the homogeneous phosphine solution. The reddish-brown color of the BrCl solution disappeared instantaneously as it was added. An orange color persisted during the addition of the last 0.5 mL, indicating total conversion. The reaction mixture was allowed to stand for 30 minutes at room temperature and then was quenched with a few drops of sodium sulfite solution which totally decolorized it. Dilution with EDC (100 mL) and washing with water (100 mL) was followed by phase separation. The organic layer was dried (Na2SO4) and concentrated to afford 2.64 g (95% yield) of triphenylphospine oxide as a white solid in 97% purity (3% starting material).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05900512
Source datasetuspto-grants-1999_05
ORD IDord-d06bbdedcbf44e4886eb5e25468b6aa5
Source noteuspto-grants-1999_05