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HRID 1463448생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1463448

반응식

참여 물질

역할이름HCID투입량
반응물3-Hydroxypicolinic AcidHCID 13401—
반응물Thionyl ChlorideHCID 24386—
반응물N,N-dimethylhydroxylamine hydrochlorideHCID 27969—
반응물DimethylhydroxylamineHCID 27970—
용매WaterHCID 962—
용매PyridineHCID 1049—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물3-hydroxy-2-(N,N-dimethylaminooxycarbonyl)pyridineHCID 19090481—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05300640
출처 데이터셋uspto-grants-1994_04
ORD IDord-be722900306f43369bf3d888b78e06c0
출처 메모uspto-grants-1994_04