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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921868Generated: October 30, 2026

Triphenylphosphonium bromide → [2-(2-Chlorobenzyloxy)-5-fluorobenzyl]triphenylphosphonium bromide

https://huagongshe.com/reaction/1921868

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphonium bromideHCID 80811—
Reactant2-(2-Chlorobenzyloxy)-5-fluorobenzyl alcoholHCID 57864329—
SolventAcetonitrileHCID 6342—
Product[2-(2-Chlorobenzyloxy)-5-fluorobenzyl]triphenylphosphonium bromideHCID 86634289—

Reaction Steps

4.60 g (17 mmol) of 2-(2-chlorobenzyloxy)-5-fluorobenzyl alcohol are dissolved in 10 ml of acetonitrile, then 5.62 g (16 mmol) of triphenylphosphine hydrobromide are added, and the suspension is stirred under reflux for 12 h. A further 2.80 g (8 mmol) of triphenylphosphine hydrobromide are added, and the mixture is stirred under reflux for a further 3 h. The solvent is mostly distilled out in vacuo, the crystals which have separated out are stirred with petroleum ether, filtered off with suction and dried on a clay dish. 9.82 g (15.7 mmol, 92% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173704B2
Source datasetuspto-grants-2012_05
ORD IDord-f099c4c3604a45d9a237cfcf4addd789
Source noteuspto-grants-2012_05