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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712662Generated: October 30, 2026

Benzyl Bromide → 3-(Benzyloxy)-5-bromopyridine

https://huagongshe.com/reaction/712662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Bromo-5-hydroxypyridineHCID 599529—
SolventAcetonitrileHCID 6342—
Product3-(Benzyloxy)-5-bromopyridineHCID 1538919834.7%

Reaction Steps

To a suspension of 5-bromo-pyridin-3-ol (1.9 g, 10.9 mmol) in acetonitrile (152 mL) is added bromomethyl-benzene (2.1 g, 12.0 mmol) and potassium carbonate (4.5 g, 32.8 mmol). The resultant mixture is stirred at room temperature for 16 h. The crude product is purified by silica gel column to afford 3-benzyloxy-5-bromo-pyridine (1.0 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181272B2
Source datasetuspto-grants-2015_11
ORD IDord-b7910708363c46bd82aa60c94a64f8b7
Source noteuspto-grants-2015_11