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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32390Generated: October 27, 2026

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

https://huagongshe.com/reaction/32390

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 numberUS07427631B2
Source datasetuspto-grants-2008_09
ORD IDord-bf5bf24fe7e74cbb812408a8fd3e4b8b
Source noteuspto-grants-2008_09