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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1864751Generated: October 29, 2026

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

https://huagongshe.com/reaction/1864751

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-Chloro-5-hydroxypyridineHCID 819821—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Product5-(Benzyloxy)-2-chloropyridineHCID 1001371788%

Reaction Steps

Sodium hydride (55% in oil, 236 mg, 5.40 mmol) washed in Hexane and 2-Chloro-5-hydroxypyridine (350 mg, 2.70 mmol) was suspended in dry DMF (20 ml). After 10 minutes at room temperature Benzylbromide (0.32 ml, 2.70 mmol) was added and the mixture was stirred for an additional 2 hrs. The reaction was diluted with water and extracted with EtOAc (3*50 ml). The combined organic layers were washed with water and brine, and dried over Na2SO4. The solvent was removed by rotary evaporation, affording 520 mg (88%) of the title compound as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625934B2
Source datasetuspto-grants-2009_12
ORD IDord-eb8e7ef0e5e74c9d96b2013f5d58790d
Source noteuspto-grants-2009_12