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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81838Generated: October 25, 2026

Pyridine → N-Methoxy-N-methylbutyramide

https://huagongshe.com/reaction/81838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantButyryl chlorideHCID 8855—
ReactantMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-Methoxy-N-methylbutyramideHCID 1370454389.6%

Reaction Steps

Pyridine (100 mL) was cooled to 0° C., and N,O-dimethylhydroxylamine hydrochloride (20.14 g, 206 mmol) was added with stirring. This solution was stirred for 10 minutes, and then a solution of butyryl chloride (19.5 ml, 20 g, 188 mmol) dissolved in 50 ml methylene chloride was added via addition funnel over 30 minutes. A precipitate formed after 5 minutes. This suspension was stirred and allowed to warm to room temperature. Stirring was continued for 2.0 hours, and the reaction was diluted with water, extracted with methylene chloride twice. The methylene chloride layers were combined and washed with 1 N HCl twice and once with brine. Diethyl ether (100 mL) was added to facilitate emulsion separation, and the organic layer was separated and washed with saturated bicarbonate solution, brine, and dried over magnesium sulfate. The solution was filtered and the solvent removed in vacuo to give N-Methoxy-N-methyl-butyramide as an oil (22.1 g, 89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846705B2
Source datasetuspto-grants-2014_09
ORD IDord-4e2ee6e098864000b4f5366db6ece7ce
Source noteuspto-grants-2014_09