Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Nitric Acid | HCID 944 | — |
| Edukt | 2-Hydroxy-5-methoxybenzaldehyde | HCID 95695 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 2-Hydroxy-5-methoxy-3-nitrobenzaldehyde | HCID 522218 | 40,5% |
Reaktionsschritte
First, 8.0 g (52.6 mmol) of 5-methoxysalicylaldehyde 5 was dissolved in 50 ml of acetic acid. Then, a mixed solution of 2.5 ml (59.7 mmol) of fuming nitric acid (99%, specific gravity 1.52) and 8 ml of acetic acid was added dropwise into the above mixture over a period of 1 hour while maintaining the temperature of the reaction mixture at approximately 15° C. with ice-cold water and strongly agitating the reaction mixture. Agitation was further continued for 7 hours. The precipitate formed was filtered, after which the precipitate was recrystallized from 500 ml of ethanol, thereby obtaining 4.2 g (21.3 mmol, yield 40.5%) of 3-nitro-5-methoxysalicylaldehyde 6 in the form of yellow needle crystals. This reaction can be expressed by the following chemical equation: ##STR7##
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05155230 |
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| Quelldatensatz | uspto-grants-1992_10 |
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| ORD ID | ord-2052b12a97224c04ae489bf0ceb1aef4 |
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| Quellennotiz | uspto-grants-1992_10 |
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