HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2421Erstellt: 23. Oktober 2026
4-Nitrobenzoic Acid → N-(2-methoxyphenyl)-4-nitrobenzamide
https://huagongshe.com/de/reaction/2421
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Nitrobenzoic Acid | HCID 6108 | — |
| Edukt | 2-Methoxyaniline | HCID 7000 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-(2-methoxyphenyl)-4-nitrobenzamide | HCID 774513 | 87,5% |
Reaktionsschritte
With cooling in an ice bath, 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC.HCl) (630 mg, 3.29 mmol) was added to 15 ml of methylene chloride solution containing o-anisidine (368 mg, 2.99 mmol) and 4-nitrobenzoic acid (500 mg, 2.99 mmol). After 1 hour of stirring at the same temperature, the reaction mixture was roughly adjusted to pH 8 with saturated sodium bicarbonate aqueous solution, extracted with methylene chloride and then washed with water and saturated brine in that order. After drying on anhydrous magnesium sulfate, the solvent was removed by evaporation, and the resulting solid material was purified by silica gel column chromatography (methylene chloride) to obtain 712 mg (87.4%) of the title compound in the form of yellow powder.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05728835 |
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| Quelldatensatz | uspto-grants-1998_03 |
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| ORD ID | ord-c4ba4a81e15b4995a5093c01878efc4c |
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| Quellennotiz | uspto-grants-1998_03 |
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