Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | N-(4-formyl-2-nitrophenyl)acetamide | HCID 291355 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 4-Amino-3-nitrobenzaldehyde | HCID 13237703 | 98% |
Reaktionsschritte
4-Acetamido-3-nitrobenzaldehyde (2.08 g, 10 mmol) was dissolved in methanol (200 mL). The solution was added with aqueous 2 N HCl (50 mL), and refluxed by heating at 80° C. for 8 hours under an argon flow. The reaction mixture was concentrated under reduced pressure to remove the methanol, and the residue was made basic with aqueous 2 N NaOH, and extracted 5 times with dichloromethane. The organic phases were combined, dried over anhydrous Na2SO4, and concentrated under reduced pressure to obtain the target compound as yellow solid (1.62 g, yield: 98%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08673957B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-a3789caf9ded4a6d987a5ba0fdfd8cfa |
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| Quellennotiz | uspto-grants-2014_03 |
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