HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075419Generated: October 30, 2026
Triphenylphosphine → Triphenylphosphine Oxide
https://huagongshe.com/reaction/1075419
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Phosphine | HCID 24404 | — |
| Reactant | BROMINE CHLORIDE (BrCl) | HCID 61697 | — |
| Reactant | HCID 22134543 | HCID 22134543 | — |
| Product | Triphenylphosphine Oxide | HCID 13097 | 95% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05900512 |
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| Source dataset | uspto-grants-1999_05 |
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| ORD ID | ord-d06bbdedcbf44e4886eb5e25468b6aa5 |
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| Source note | uspto-grants-1999_05 |
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