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HRID 893515作成日:2026年10月26日

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

https://huagongshe.com/reaction/893515

反応式

関与物質

役割名称HCID仕込み量
反応物3-Hydroxypicolinic AcidHCID 13401—
反応物Thionyl ChlorideHCID 24386—
反応物N,N-dimethylhydroxylamine hydrochlorideHCID 27969—
反応物DimethylhydroxylamineHCID 27970—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
溶媒TriethylamineHCID 8471—
生成物3-hydroxy-2-(N,N-dimethylaminooxycarbonyl)pyridineHCID 19090481—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05125957
出典データセットuspto-grants-1992_06
ORD IDord-d0296fcd6cf8468693e7e5b12c93b47c
出典メモuspto-grants-1992_06