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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85221Generated: October 25, 2026

Triphenylphosphine → (2-Fluoro-5-nitrobenzyl)(triphenyl)phosphonium bromide

https://huagongshe.com/reaction/85221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant2-(Bromomethyl)-1-fluoro-4-nitrobenzeneHCID 10353967—
SolventTolueneHCID 1140—
Product(2-Fluoro-5-nitrobenzyl)(triphenyl)phosphonium bromideHCID 86643536—

Reaction Steps

20 g (85.5 mmol) of the compound from Example 26A are dissolved in 250 ml of anhydrous toluene, and 22.4 g (85.5 mmol) of triphenylphosphine are added. The solution is heated under reflux for 16 h, resulting in the formation of a precipitate. The mixture is allowed to cool, and the precipitate is filtered off. After washing with diethyl ether, the precipitate is dried under reduced pressure. This gives 39 g (92% of theory) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846934B2
Source datasetuspto-grants-2014_09
ORD IDord-26f40b40097c47ada2414ad639ecf279
Source noteuspto-grants-2014_09