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HRID 1463448Erstellt: 25. Oktober 2026

3-Hydroxypicolinic Acid → 3-hydroxy-2-(N,N-dimethylaminooxycarbonyl)pyridine

https://huagongshe.com/reaction/1463448

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Hydroxypicolinic AcidHCID 13401—
EduktThionyl ChlorideHCID 24386—
EduktN,N-dimethylhydroxylamine hydrochlorideHCID 27969—
EduktDimethylhydroxylamineHCID 27970—
LösungsmittelWaterHCID 962—
LösungsmittelPyridineHCID 1049—
LösungsmittelChloroformHCID 6212—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTriethylamineHCID 8471—
Produkt3-hydroxy-2-(N,N-dimethylaminooxycarbonyl)pyridineHCID 19090481—

Reaktionsschritte

7.0 Grams of 3-hydroxypicolinic acid was dissolved in 10 ml of N,N-dimethylformamide, and the resulting solution was cooled to 0° to 5° C. 5.9 Grams of thionyl chloride was then added dropwise to the solution which was then stirred at 0° to 5° C. for further 30 minutes. Thereafter, 30 ml of chloroform was added to the solution which was then stirred at 0° to 5° C. for further 15 minutes. To the resulting mixed solution was added dropwise a dichloromethane solution of N,N-dimethylhydroxylamine prepared from 7.4 g of N,N-dimethylhydroxylamine hydrochloride and 7.6 g of triethylamine. After stirring at 0° to 5° C. for 30 minutes, 7.9 g of pyridine was added, and stirring was continued at 0° to 5° C. for further 1 hour. After stirring at room temperature for 8 hours, the reaction solution was poured into water, and insoluble matters were removed by filtration on celite. The organic layer was washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue obtained was subjected to chromatography to obtain 1.0 g of 3-hydroxy-2-(N,N-dimethylaminooxycarbonyl)pyridine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05300640
Quelldatensatzuspto-grants-1994_04
ORD IDord-be722900306f43369bf3d888b78e06c0
Quellennotizuspto-grants-1994_04