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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 70713Generated: October 28, 2026

4-Methyloxybenzyl chloride → HCID 86658014, compound

https://huagongshe.com/reaction/70713

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methyloxybenzyl chlorideHCID 69993—
ReactantAluminumHCID 5359268—
Reactant5-Cyclopropyl-6-oxo-1,6-dihydropyridine-2-carbaldehydeHCID 86658013—
CatalystHCID 178418647HCID 178418647—
SolventChloroformHCID 6212—
ProductHCID 86658014HCID 86658014105.3%

Reaction Steps

p-Methoxybenzyl chloride (329 mg) was added to a solution of 5-cyclopropyl-6-oxo-1,6-dihydropyridine-2-carbaldehyde (228 mg) in chloroform (10 mL), after which the reaction tube was covered with aluminum foil to provide shading conditions. Silver carbonate (771 mg) was added and the mixture was stirred at room temperature for three hours. The insoluble matter was filtered off and then the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=92:8→34:66) to give 5-cyclopropyl-6-[(4-methoxybenzyl)oxy]pyridine-2-carbaldehyde as a colorless oil (417 mg, 86%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822503B2
Source datasetuspto-grants-2014_09
ORD IDord-c572a8a4b46340c5917b7d7882651cf1
Source noteuspto-grants-2014_09