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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38423Erstellt: 23. Oktober 2026

Pyridine → N-Methoxy-N-methylbutyramide

https://huagongshe.com/de/reaction/38423

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPyridineHCID 1049—
EduktButyryl chlorideHCID 8855—
EduktMethanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
LösungsmittelWaterHCID 962—
LösungsmittelDichloromethaneHCID 6344—
ProduktN-Methoxy-N-methylbutyramideHCID 1370454389,6%

Reaktionsschritte

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%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08524725B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-109e15bc209b40dfb5e8718fff1ed275
Quellennotizuspto-grants-2013_09