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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970091Generated: October 30, 2026

Hydrochloric Acid → Triphenylphosphine

https://huagongshe.com/reaction/1970091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriphenylphosphine OxideHCID 13097—
ReactantLead (II) bromideHCID 24831—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminumHCID 5359268—
SolventAcetonitrileHCID 6342—
ProductTriphenylphosphineHCID 1177688%
ProductTriphenylphosphine OxideHCID 130972%

Reaction Steps

Triphenylphosphine oxide (1.40 g, 5.0 mmol), shredded aluminum foil (136 mg, 5.0 mmol) and acetonitrile (5 mL) were weighted out into a reactor, then oxalyl chloride (0.46 mL, 5.1 mmol) was added thereto under room temperature, and the mixture was stirred at the same temperature for 10 minutes. Subsequently, lead bromide (18 mg, 0.05 mmol) was added to this reaction solution, and the mixture was stirred for 30 minutes at room temperature. Thereafter, the reaction solution was poured into an iced 5% hydrochloric acid aqueous solution from the reactor, to terminate the reaction. 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 (1,162 mg, 4.4 mmol, yield: 88%) and triphenylphosphine oxide (21 mg, 0.07 mmol, collection rate: 2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426629B2
Source datasetuspto-grants-2013_04
ORD IDord-5a0be7df485a470b87ff2000ca9e55a1
Source noteuspto-grants-2013_04