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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436348Generated: October 29, 2026

Triphenylphosphine Oxide → Triphenylphosphine

https://huagongshe.com/reaction/436348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphine OxideHCID 13097—
ReactantSilicon tetrachlorideHCID 24816—
ReactantHCID 178418361HCID 178418361—
CatalystSulfurHCID 5362487—
ProductTriphenylphosphineHCID 1177686.9%

Reaction Conditions

Temperature250 °C

Reaction Steps

To an oven-dried 50-ml autoclave liner were added 16.68 g of triphenylphosphine oxide (.06 mole) and 0.057 g of sulfur (.0018 mole). The solids were treated with 11.12 g of silicon tetrachloride (.066 mole) and the mixture was placed in an autoclave which was then charged to a pressure of 715 p.s.i.g. (48 atm.) with hydrogen. The mixture was heated to 250°C for 15 hours at a maximum pressure of 77 atm. After cooling and venting, the reaction mixture was worked up by first partitioning between warm 30% by weight aqueous sodium hydroxide solution and toluene. The aqueous layer was extracted once with toluene and the combined organic layers were washed with water and with brine and dried over anhydrous sodium sulfate. Filtration and solvent removal gave 13.66 g (86.9%) of crude triphenylphosphine, mp 68°-77° which contained 2% triphenylphosphine oxide and 3% triphenylphosphine sulfide by gas-liquid chromatographic (glc) analysis. Recrystallization from methanol gave 11.25 g (71%) of purified triphenylphosphine, mp 75°-9°, still containing 1-2% triphenylphosphine sulfide by glc analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04008282
Source datasetuspto-grants-1977_02
ORD IDord-dd467331b3034d818264ef285eb2b622
Source noteuspto-grants-1977_02