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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269581Generated: October 29, 2026

Benzyl Bromide → 2-(Benzyloxy)-3-bromo-5-chloropyridine

https://huagongshe.com/reaction/269581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 178517755HCID 178517755—
CatalystHCID 178418647HCID 178418647—
SolventTolueneHCID 1140—
Product2-(Benzyloxy)-3-bromo-5-chloropyridineHCID 22058382—

Reaction Steps

3-Bromo-5-chloro-2-pyridinol (7.0 g, 33.6 mmol) was stirred in toluene (160 ml) and silver carbonate (10.23 g, 36.9 mmol) added, followed by benzyl bromide (6.32 g, 4.39 ml, 36.9 mmol). The mixture was heated to reflux for 1 hour. After cooling, the mixture was filtered, washed with water (×2), dried (MgSO4) and evaporated. The residue was triturated with isohexane and the pale yellow solid filtered and dried. (8.36 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07446222B2
Source datasetuspto-grants-2008_11
ORD IDord-d4369e9f678b4d7381f563c85bf92a92
Source noteuspto-grants-2008_11