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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1588428Generated: November 4, 2026

Triphenylphosphine → 2-{3-[3-(4-Fluorophenoxy)propoxy]phenyl}-ethyl triphenylphosphonium bromide

https://huagongshe.com/reaction/1588428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-{3-[3-(4-Fluorophenoxy)propoxy]phenyl}-ethyl bromideHCID 19755708—
SolventEthanolHCID 702—
Product2-{3-[3-(4-Fluorophenoxy)propoxy]phenyl}-ethyl triphenylphosphonium bromideHCID 8674500850%

Reaction Steps

A solution of 20 mmol of bromide (example 141) and 30 mmol of triphenyl phosphine in 60 ml of ethanol was refluxed 20 hours under nitrogen and then cooled and evaporated in vacuo. The residue was chromatographed on silica gel using first CHCl3 to elute starting material residues and then 5% CH3OH in CHCl3 to elute the product. Evaporation of pure fractions yielded the title compound as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05221760
Source datasetuspto-grants-1993_06
ORD IDord-9dcf4ded112e40e487feafda66fef6d6
Source noteuspto-grants-1993_06