Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 917774Generated: November 1, 2026

Dimethyl Sulfate → Ethyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylate

https://huagongshe.com/reaction/917774

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfateHCID 6497—
ReactantEthyl 4,6-dichloropyridine-3-carboxylateHCID 600045—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
SolventSodium BicarbonateHCID 516892—
ProductEthyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridine-3-carboxylateHCID 1161545185%

Reaction Conditions

Temperature120 °C

Reaction Steps

Ethyl 4,6-dichloronicotinate [prepared according to the literature procedure of J. Chem. Soc. 5163 (1963)] (3.19 g, 14.5 mmol) and dimethyl sulfate (6.0 mL, 63 mmol) were combined in a thick-walled glass tube with a Teflon cap. The tube was sealed and heated in a 120° C. sand bath. After 5 h, the reaction was cooled to ambient temperature and diluted with acetonitrile (100 mL) and saturated aqueous sodium bicarbonate solution (100 mL). The reaction mixture was stirred vigorously overnight (ca. 18 h). This mixture was further diluted with water and extracted with dichloromethane (3×). The combined extracts were washed with brine, dried over anhydrous magnesium sulfate and concentrated in vacuo to afford 4-chloro-1-methyl-6-oxo-1,6-dihydro-pyridine-3-carboxylic acid ethyl ester (2.65 g, 85% yield) as an oil that solidified upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07273877B2
Source datasetuspto-grants-2007_09
ORD IDord-fa2f21dc32a340cba478e1aed4a40b6d
Source noteuspto-grants-2007_09