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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1164656Generated: October 31, 2026

4-Nitrobenzyl bromide → 2-(Benzylsulfanyl)-1-[(4-nitrophenyl)methyl]pyridin-1-ium bromide

https://huagongshe.com/reaction/1164656

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzyl bromideHCID 66011—
Reactant2-benzylsulfanylpyridineHCID 472961—
SolventAcetoneHCID 180—
Product2-(Benzylsulfanyl)-1-[(4-nitrophenyl)methyl]pyridin-1-ium bromideHCID 13435003—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 4-nitrobenzyl bromide (1.08 g) and 2-(benzylthio)pyridine (1.05 g) were heated at 100° C. for 4 hours and cooled. Crystals which formed on trituration with acetone were removed by filtration and dried to give the title compound as a quarter hydrate (1.6 g) mp 160°-2° C. (Found C, 53.8; H, 4.5; N, 6.4%. C19H17BrN2O2S1/4H2O requires C, 54.1; H, 4.2; N, 6.6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04370477
Source datasetuspto-grants-1983_01
ORD IDord-ab26f00d6e0d4bc09df041ae57b4f64f
Source noteuspto-grants-1983_01