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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 2-Chloro-3-nitrobenzoic acid | HCID 19870 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Edukt | N-methylhydroxylamine hydrochloride | HCID 77906 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | N-methyl-N-hydroxy-2-chloro-3-nitrobenzamide | HCID 18706122 | 89,5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06080702 |
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| Quelldatensatz | uspto-grants-2000_06 |
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| ORD ID | ord-508616ff3d344431965cb4b8d09d056a |
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| Quellennotiz | uspto-grants-2000_06 |
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