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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1421848Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1421848

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Chloro-3-nitrobenzoic acidHCID 19870—
EduktThionyl ChlorideHCID 24386—
EduktN-methylhydroxylamine hydrochlorideHCID 77906—
EduktSodium BicarbonateHCID 516892—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
LösungsmittelDiethyl EtherHCID 3283—
ProduktN-methyl-N-hydroxy-2-chloro-3-nitrobenzamideHCID 1870612289,5%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06080702
Quelldatensatzuspto-grants-2000_06
ORD IDord-508616ff3d344431965cb4b8d09d056a
Quellennotizuspto-grants-2000_06