HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1633718Erstellt: 24. Oktober 2026
4-Methoxy-3-nitrobenzaldehyde → Ethanol, reaction products with ammonia, distn. residues
https://huagongshe.com/de/reaction/1633718
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Methoxy-3-nitrobenzaldehyde | HCID 700608 | — |
| Edukt | N,N-Dimethyl 4-iodo-1H-imidazole-1-sulfonamide | HCID 2773390 | — |
| Edukt | HCID 178418443 | HCID 178418443 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | Ethanol, reaction products with ammonia, distn. residues | HCID 22020343 | 20% |
| Produkt | HCID 178491310 | HCID 178491310 | — |
Reaktionsschritte
A solution of 4-iodo-N,N-dimethyl-1H-imidazole-1-sulfonamide (3.0 g, 10 mmol) in dichloromethane (40 mL) under nitrogen was treated with ethylmagnesium bromide (3.0 M in diethyl ether, 3.3 mL) over 2 minutes, stirred for 30 minutes, treated with 4-methoxy-5-nitrobenzaldehyde (2.0 g, 11 mmol), stirred for 1 hour, stored at 0° C. for 16 hours, concentrated to dryness, treated with 1M HCl(100 mL), heated to 100° C. for 16 hours, cooled to ambient temperature, neutralized with NaHCO3 and extracted with 3:1 dichloromethane:ethanol (5×). The combined extractions were dried (MgSO4), filtered and concentrated. Purification on silica gel with 10% and then 20% ethanol/ammonia-saturated dichloromethane provided the desired compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06503935B1 |
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| Quelldatensatz | uspto-grants-2003_01 |
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| ORD ID | ord-cc3d2391fc2842d9833404e6d64bd57c |
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| Quellennotiz | uspto-grants-2003_01 |
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