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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1420716Generated: November 2, 2026

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

https://huagongshe.com/reaction/1420716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantHCID 178517755HCID 178517755—
CatalystHCID 178418647HCID 178418647—
SolventBenzeneHCID 241—
Product2-(Benzyloxy)-3-bromo-5-chloropyridineHCID 22058382—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 3-bromo-5-chloro-2-hydroxypyridine (81 g), benzyl bromide (52 mL) and silver carbonate (97 g) in benzene (1 L) was heated at 70° C. for 1 h. The mixture was cooled to r.t. and then filtered through a bed of celite. The filtrate was concentrated and the residual off-white solid was recrystallized from hexane to provide the title compound as a white solid (102 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06071936
Source datasetuspto-grants-2000_06
ORD IDord-b4f4b0fca9db49098d89db98cdde5ca9
Source noteuspto-grants-2000_06