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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970094Generated: November 1, 2026

Hydrochloric Acid → Triphenylphosphine

https://huagongshe.com/reaction/1970094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriphenylphosphine OxideHCID 13097—
ReactantOxalyl chlorideHCID 65578—
ReactantAluminumHCID 5359268—
SolventAcetonitrileHCID 6342—
ProductTriphenylphosphineHCID 1177693%
ProductTriphenylphosphine OxideHCID 130973%

Reaction Steps

Triphenylphosphine oxide (1.401 g, 5.0 mmol) and acetonitrile (5 mL) were weighted out into a reactor containing the granular aluminum collected after the first reaction, then oxalyl chloride (0.46 mL, 5.10 mmol) was added thereto under room temperature, and the mixture was stirred for 1 hour to cause a reaction. The reaction solution was taken out with a syringe and poured into an iced 5% hydrochloric acid aqueous solution, and further, the granular aluminum was washed with ethyl acetate, and a wash liquid was also poured into the iced 5% hydrochloric acid aqueous solution as well. 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 (1.23 g, 4.67 mmol, yield: 93%) and triphenylphosphine oxide (40 mg, 0.14 mmol, collection rate: 3%) (second reaction).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426629B2
Source datasetuspto-grants-2013_04
ORD IDord-c2f32da8963647fd8b930bd9f4a54866
Source noteuspto-grants-2013_04