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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466163Generated: October 31, 2026

Triethylamine → 6-Benzoyloxy-2-(4-bromobenzoyloxy)-3-cyanopyridine

https://huagongshe.com/reaction/466163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Bromobenzoyl chlorideHCID 68515—
ReactantHCID 178510098HCID 178510098—
Solvent1,4-DioxaneHCID 31275—
Product6-Benzoyloxy-2-(4-bromobenzoyloxy)-3-cyanopyridineHCID 1404963984.6%

Reaction Steps

Triethylamine (3.46 ml) and 1.82 g of 4-bromobenzoyl chloride were added to a solution of 2.00 g of 6-benzoyloxy-3-cyano-2-hydroxypyridine in 50 ml of dioxane. The mixture was stirred at room temperature for 1 hour. The salt thus produced was separated by filtration and the filtrate was concentrated. The concentrate was applied to silica gel column chromatography using, as an eluent, chloroform, giving 2.97 g of the title compound in a yield of 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155113
Source datasetuspto-grants-1992_10
ORD IDord-1e9698ab616546c7bf5277b6b970ac44
Source noteuspto-grants-1992_10