Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570829Generated: October 26, 2026

Benzyl Alcohol → 5-Benzyloxy-2-bromoisonicotinic acid ethyl ester

https://huagongshe.com/reaction/570829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantHCID 46311464HCID 46311464—
SolventTetrahydrofuranHCID 8028—
Product5-Benzyloxy-2-bromoisonicotinic acid ethyl esterHCID 8664516661.1%

Reaction Steps

To a solution of benzylalcohol (1.5 g) in tetrahydrofuran (30 mL) was added sodium hydride (55%, 0.3 g) under ice cooling, and this mixture was stirred at same temperature for 5 minutes. To this reaction mixture was added a solution of 2-bromo-5-fluoroisonicotinic acid ethyl ester (2.9 g) in tetrahydrofuran (30 mL), and this mixture was stirred at room temperature for 2 hours. This reaction mixture was poured into water, and this mixture was extracted with ethyl acetate. This organic layer was washed with water and brine, dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: ethyl acetate/n-hexane) to give the title compound (2.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023882B2
Source datasetuspto-grants-2015_05
ORD IDord-bf0d40ada5fa4aa89b056549407ce9fc
Source noteuspto-grants-2015_05