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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1672655Generated: October 27, 2026

Triphenylphosphonium hydrobromide → {5-Fluoro-2-[2-(4-trifluoromethylphenyl)ethoxy]benzyl}triphenylphosphonium bromide

https://huagongshe.com/reaction/1672655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphonium hydrobromideHCID 22178555—
Reactant5-Fluoro-2-[2-(4-trifluoromethylphenyl)ethoxy]benzyl alcoholHCID 57864413—
SolventAcetonitrileHCID 6342—
Product{5-Fluoro-2-[2-(4-trifluoromethylphenyl)ethoxy]benzyl}triphenylphosphonium bromideHCID 8663429182.5%

Reaction Steps

1.7 g (5.41 mmol) of {5-fluoro-2-[2-(4-trifluoromethylphenyl)ethoxy]phenyl}methanol and 1.76 g (5.14 mmol) of triphenylphosphonium hydrobromide are heated under reflux in 20 ml of acetonitrile for three hours. A first product fraction is crystallized at −20° C. The mother liquor is concentrated, the residue is dissolved in dichloromethane, and a second fraction is crystallized with diethyl ether. A total of 2.71 g (76% yield) of the title compound is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07998988B2
Source datasetuspto-grants-2011_08
ORD IDord-25124effb83040bf96eac9300a88a2d8
Source noteuspto-grants-2011_08