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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963558Generated: November 1, 2026

Tributylphosphine → [2-(3-Butenyloxy)ethyl]benzene

https://huagongshe.com/reaction/963558

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant2-Nitrophenyl selenocyanateHCID 103931—
Reactant4-Phenethoxybutan-1-olHCID 19082188—
SolventTetrahydrofuranHCID 8028—
Product[2-(3-Butenyloxy)ethyl]benzeneHCID 1293682992%

Reaction Steps

To a solution of 4-[2-phenylethoxy]butanol (3.16 g) and 2-nitrophenyl selenocyanate (4.0 g) in THF (50 ml) under argon was added tributylphosphine (4.5 ml) in THF (2 ml) dropwise over 30 min. After a further 2 hours at room temperature the solvent was removed under reduced pressure. A further 50 ml of THF was added and the mixture cooled to 0° at which point H2O2 (17 ml, 30% aqueous v/v) was added to the stirred solution over 1 hour. The mixture was allowed to warm to room temperature and stirring continued overnight. The solvent was removed under reduced pressure and the residue taken up in ether, washed with 1 molar aqueous hydrochloric acid, sodium bicarbonate solution and brine. The solution was dried, filtered and the solvent removed under reduced pressure to yield a yellow oil which was purified by chromatography using diethyl ether in petroleum ether (bp 60°-80°) as eluant to yield the subtitled compound (2.63 g, 92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05763465
Source datasetuspto-grants-1998_06
ORD IDord-8f8736cd073a4183b6287bb57b8da5db
Source noteuspto-grants-1998_06