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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922062Generated: October 31, 2026

m-Chloroperbenzoic acid → 6-Chloro-2,4-diethyl-pyridine-3-carboxylic acid ethylester

https://huagongshe.com/reaction/922062

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantEthyl 2,4-diethylpyridine-3-carboxylateHCID 59589505—
SolventChloroformHCID 6212—
Product6-Chloro-2,4-diethyl-pyridine-3-carboxylic acid ethylesterHCID 8666433749.7%

Reaction Steps

To a solution of 2.73 g (14.12 mmol) 2,4-diethyl-pyridine-3-carboxylic acid ethylester in chloroform (109 ml) was added 6.97 g, (70% pure, 28.29 mmol) mCPBA at 0° C. The reaction mixture was stirred at RT for 6 h and was then diluted with chloroform and washed with a sat. NaHCO3 sol and brine. The organic layer was dried over Na2SO4 and concentrated in vacuo. The residue was dissolved in POCl3 (70 ml) and the reaction mixture was heated at 110° C. for 6.5 h. Then excess POCl3 was evaporated and cold water was added to the residue. The mixture was basified with a sat. NaHCO3 sol to pH˜10 and was extracted EtOAc. The organic layer was washed with water and brine, dried over Na2SO4 and concentrated in vacuo. Purification of this residue by CC (hexane/EtOAc 9:1) provided 1.6 g (7.02 mmol, 20%) 6-chloro-2,4-diethyl-pyridine-3-carboxylic acid ethylester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278103B2
Source datasetuspto-grants-2016_03
ORD IDord-b1dcc2227d2a424fbdb72c2fd3626e95
Source noteuspto-grants-2016_03