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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 247919Generated: October 26, 2026

Benzyl Bromide → 2-[[Acetyl[4-(tetradecyloxy)benzoyl]amino]methyl]-1-(phenylmethyl)pyridinium bromide

https://huagongshe.com/reaction/247919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantN-Acetyl-N-(2-pyridinylmethyl)-4-(tetradecyloxy)benzamideHCID 11754296—
SolventAcetonitrileHCID 6342—
Product2-[[Acetyl[4-(tetradecyloxy)benzoyl]amino]methyl]-1-(phenylmethyl)pyridinium bromideHCID 1046176550.2%

Reaction Steps

A mixture of 0.75 g of product from Example 5, 0.412 g of benzyl bromide and 3 ml of acetonitrile is stirred at room temperature for 17.5 hours then heated, in a sealed tube, at 100° C. for 21.25 hours. The cooled reaction mixture is concentrated in vacuo and the residue purified by column chromatography (silica gel: 10% methyl alcohol/chloroform) to give 0.515 g of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05208247
Source datasetuspto-grants-1993_05
ORD IDord-278fac69d2954beea6dae9c36d44ea40
Source noteuspto-grants-1993_05