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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365261Generated: October 29, 2026

Benzyl Bromide → HCID 58368201, compound

https://huagongshe.com/reaction/2365261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantMethyl 6-oxo-1,6-dihydropyridine-3-carboxylateHCID 416343—
ReactantAluminumHCID 5359268—
CatalystHCID 178418647HCID 178418647—
SolventBenzeneHCID 241—
SolventEthyl AcetateHCID 8857—
ProductHCID 58368201HCID 58368201—

Reaction Steps

To a solution of methyl 6-oxo-1,6-dihydropyridine-3-carboxylate (2.00 g, 13.1 mmol) in 45 mL of benzene was added benzyl bromide (1.86 mL, 15.7 mmol) and silver carbonate (3.96 g, 14.4 mmol). The flask was covered with aluminum foil, and after 85 hr, the mixture was diluted with ethyl acetate, filtered through celite, and concentrated in vacuo. The residue was purified via silica gel chromatography, eluting with 0-20% ethyl acetate in hexanes to provide methyl 6-(benzyloxy)pyridine-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697690B2
Source datasetuspto-grants-2014_04
ORD IDord-137ab7a07a0d424bbe37ae382baedb39
Source noteuspto-grants-2014_04