HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970092Generated: October 31, 2026
Hydrochloric Acid → Triphenylphosphine Oxide
https://huagongshe.com/reaction/1970092
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triphenylphosphine Oxide | HCID 13097 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Triphenylphosphine | HCID 11776 | 4% |
| Product | Triphenylphosphine Oxide | HCID 13097 | 94% |
Reaction Steps
Triphenylphosphine oxide (1.405 g, 5.0 mmol) and acetonitrile (5 mL) were weighted out into a reactor, then oxalyl chloride (0.43 mL, 5.05 mmol) was added thereto under room temperature, and the mixture was stirred for 10 minutes. Then, previously shredded aluminum foil (135 mg, 5.0 mmol) was added to this reaction solution, and subsequently the mixture was stirred for 1 hour under room temperature to cause a reaction. The reaction solution was poured into an iced 5% hydrochloric acid aqueous solution from the reactor, to terminate the reaction, and thereafter the organic layer was separated, and the water layer was extracted with ethyl acetate for 3 times. The organic layers were combined into one, washed with saturated saline, dried on sodium sulfate and concentrated under reduced pressure. The residue was purified with a silica gel column chromatography to give triphenylphosphine (47 mg, 0.18 mmol, yield: 4%) and triphenylphosphine oxide (1.32 g, 4.75 mmol, collection rate: 94%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08426629B2 |
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| Source dataset | uspto-grants-2013_04 |
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| ORD ID | ord-f83aeda1819848ee91395ddc9c0b4572 |
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| Source note | uspto-grants-2013_04 |
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