HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1507310Erstellt: 25. Oktober 2026
5-Bromo-1-methyl-1H-imidazole → (1-Methyl-1H-imidazol-5-yl)(3-methyl-4-nitrophenyl)methanone
https://huagongshe.com/reaction/1507310
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 5-Bromo-1-methyl-1H-imidazole | HCID 1515258 | — |
| Edukt | N-methoxy-N,3-dimethyl-4-nitrobenzamide | HCID 46318653 | — |
| Edukt | HCID 178461630 | HCID 178461630 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | (1-Methyl-1H-imidazol-5-yl)(3-methyl-4-nitrophenyl)methanone | HCID 86715615 | — |
Reaktionsschritte
A solution of EtMgBr (3.0 M in diethylether, 8.5 mL, 25.69 mmol) was added dropwise, over a 25 minute period to a solution of 5-bromo-1-methyl-1H-imidazole (4.1 g, 25.69 mmol) in dry DCM (25 mL). The mixture was stirred at room temperature for 15 minutes, cooled in an ice-brine bath and N-methoxy-N,3-dimethyl-4-nitrobenzamide (4.8 g, 21.41 mmol. Intermediate 13: step a) dissolved in 10 mL of DCM was added dropwise. A dark brown solid mass formed. The ice bath was removed and the mixture stirred at room temperature for 48 hours. Water was added to the suspension followed by 6 M aqueous HCl slowly to neutralize the mixture (pH=6-7). More DCM was added and the layers were separated. The organic layer was dried over Na2SO4, filtered and concentrated. Et2O was added, the slurry sonicated, and the precipitates filtered to provide the title compound as a tan solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09221804B2 |
|---|
| Quelldatensatz | uspto-grants-2015_12 |
|---|
| ORD ID | ord-841b15bbce4941b98c52ed10e7237997 |
|---|
| Quellennotiz | uspto-grants-2015_12 |
|---|