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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250557Generated: October 31, 2026

Pyridine → Ethyl 7-acetyl-7-(4-cyanobenzoyl)-8-oxononanoate

https://huagongshe.com/reaction/2250557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant4-Cyanobenzoyl chlorideHCID 80172—
ReactantMagnesium ChlorideHCID 5360315—
ReactantEthyl 7-acetyl-8-oxononanoateHCID 14691968—
SolventDichloromethaneHCID 6344—
ProductEthyl 7-acetyl-7-(4-cyanobenzoyl)-8-oxononanoateHCID 574445295,740.9%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a mixture of ethyl 7-acetyl-8-oxononanoate (4.0 g) and magnesium chloride (1.27 g) in dichloromethane (70 ml) was added pyridine (2.15 ml) at 0° C. The mixture was stirred at 20° C. for 1 hour, then a solution of 4-cyanobenzoyl chloride (2.87 g) in dichloromethane (10 ml) was added. After stirring for 3 hours at 20° C., the mixture was partitioned between ether and 1N hydrochloric acid. The organic layer was separated, washed with water and brine, dried over magnesium sulfate, and evaporated. The residue was chromatographed on silica gel eluting with a mixture of ethyl acetate and hexane (1:5) to give ethyl 7-acetyl-7-(4-cyanobenzoyl)-8-oxononanoate (352 g) as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317009B2
Source datasetuspto-grants-2008_01
ORD IDord-f7cd97cb465043498227ac168238cfd4
Source noteuspto-grants-2008_01