Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2406608Generated: October 29, 2026

4-Methylpyridine → 1-(2-Chlorophenyl)-2-(pyridin-4-yl)ethanone

https://huagongshe.com/reaction/2406608

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylpyridineHCID 7963—
ReactantLithium diisopropylamideHCID 2724682—
Reactant2-Chloro-N-methoxy-N-methylbenzamideHCID 18185370—
SolventTetrahydrofuranHCID 8028—
Product1-(2-Chlorophenyl)-2-(pyridin-4-yl)ethanoneHCID 1137924847%

Reaction Conditions

Temperature0 °C

Reaction Steps

To lithium diisopropyl amide (6.5 mL, 1.6 M in cyclohexane, 10.4 mmol) in THF (20.0 mL) at −78° C. was added a solution of 4-picoline (1.07 g mL, 11.5 mmol) in THF (10.0 mL) dropwise. The dry ice bath was removed. The reaction mixture was stirred at 0° C. for 30 minutes, and cooled back to −78° C. A solution of 2-chloro-N-methoxy-N-methylbenzamide (21) (2.39 g, 12 mmol) in THF (10.0 mL) was added dropwise. The reaction mixture was warmed to room temperature and stirred overnight. White solid was filtered off and dissolved in ethyl acetate. The organic phase was washed with water, brine, dried over dried magnesium sulfate and concentrated under vacuum to give 1-(2-chlorophenyl)-2-(pyridin-4-yl)ethanone (22) (1.09 g, 4.7 mmol, 47%) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08809379B2
Source datasetuspto-grants-2014_08
ORD IDord-4965e3e9edb44ff3aed2ba6d23858312
Source noteuspto-grants-2014_08