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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577457Generated: October 28, 2026

Benzyl Chloride → HCID 86723689, compound

https://huagongshe.com/reaction/577457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
Reactant4-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrileHCID 15641800—
CatalystHCID 178418778HCID 178418778—
SolventTolueneHCID 1140—
ProductHCID 86723689HCID 8672368983%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of 4-ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile (Cpd AA, 1.1 g, 6.8 mmol), (chloromethyl)benzene (1.1 mL, 9.4 mmol, 1.4 equiv) and silver(I) oxide (1.8 g, 7.7 mmol) in anhydrous toluene (22.7 mL) was heated at 110° C. for 17 hours. The reaction mixture was cooled to 23° C. then filtered through CELITE®. The filtrate was concentrated under vacuum. The residue was purified by column chromatography (heptane/EtOAc) to give 2-(benzyloxy)-4-ethyl-6-methylpyridine-3-carbonitrile (Cpd BB, 1.42 g, 83%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040515B2
Source datasetuspto-grants-2015_05
ORD IDord-45fbec9cd137473fb3784c556afecee3
Source noteuspto-grants-2015_05