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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1728805Generated: November 1, 2026

Pyridine → 1-(Bromomethyl)-4-(tetradecyloxy)benzene

https://huagongshe.com/reaction/1728805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetonitrileHCID 6342—
ReactantPhosphorus tribromideHCID 24614—
Reactant4-Tetradecyloxybenzyl alcoholHCID 10087384—
SolventDichloromethaneHCID 6344—
Product1-(Bromomethyl)-4-(tetradecyloxy)benzeneHCID 1002284088.7%

Reaction Steps

To a room temperature slurry of 2.5 g of product from Example 19, 10 ml of acetonitrile and 0.339 g of pyridine is added dropwise, over 3 minutes, 2.11 g of phosphorus tribromide. The reaction is stirred at room temperature for 1 hour, diluted with methylene chloride and concentrated in vacuo. The residue is dissolved in methylene chloride, filtered through a silica gel pad and concentrated in vacuo to give 2.65 g of the desired product as pale yellow crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05328921
Source datasetuspto-grants-1994_07
ORD IDord-081f92c8ce18482c9cf3a6cda5d18af9
Source noteuspto-grants-1994_07