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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1421848생성일: 2026년 10월 25일

2-Chloro-3-nitrobenzoic acid → N-methyl-N-hydroxy-2-chloro-3-nitrobenzamide

https://huagongshe.com/reaction/1421848

반응식

참여 물질

역할이름HCID투입량
반응물2-Chloro-3-nitrobenzoic acidHCID 19870—
반응물Thionyl ChlorideHCID 24386—
반응물N-methylhydroxylamine hydrochlorideHCID 77906—
반응물Sodium BicarbonateHCID 516892—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매Diethyl EtherHCID 3283—
생성물N-methyl-N-hydroxy-2-chloro-3-nitrobenzamideHCID 1870612289.5%

반응 단계

To a stirred solution of 2-chloro-3-nitrobenzoic acid (6.0 grams, 0.031 mole) in toluene (100 mL) was added thionyl chloride (6.8 mL, 0.092 mole). Upon completion of addition, the reaction mixture was heated to reflux where it stirred for four hours. After this time, the reaction mixture was filtered and concentrated. The concentrate was taken up in ether and added dropwise to an ice-cold solution of N-methylhydroxylamine hydrochloride (2.6 g, 0.031 mole), sodium bicarbonate (5.5 g, 0.065 mole), water (20 mL), and ether (160 mL). Upon completion of addition, the reaction mixture was stirred for one hour. After this time, the reaction mixture was diluted with water and the ether layer was separated. The aqueous layer was extracted twice with ether. The combined ether layer and extracts were dried over magnesium sulfate and concentrated to provide 6.4 grams of N-methyl-N-hydroxy-2-chloro-3-nitrobenzamide. The NMR spectrum was consistent with the proposed structure.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06080702
출처 데이터셋uspto-grants-2000_06
ORD IDord-508616ff3d344431965cb4b8d09d056a
출처 메모uspto-grants-2000_06