HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 39191Erstellt: 24. Oktober 2026
Diethyl methylmalonate → Diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate
https://huagongshe.com/de/reaction/39191
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl methylmalonate | HCID 11857 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 2-Bromo-1-fluoro-4-nitrobenzene | HCID 69699 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate | HCID 59206132 | 99% |
Reaktionsschritte
Diethyl 2-methylmalonate (4.31 mL, 25.0 mmol) was dissolved in 25 mL of anhydrous DMF. This solution was cooled to 0° C. under an atmosphere of nitrogen. Sodium hydride (1.04 g, 26 mmol, 60% by weight in mineral oil) was slowly added to the solution. The resulting mixture was allowed to stir for 3 minutes at 0° C., and then at room temperature for 10 minutes. 2-Bromo-1-fluoro-4-nitrobenzene (5.00 g, 22.7 mmol) was quickly added and the mixture turned bright red. After stirring for 10 minutes at room temperature, the crude mixture was evaporated to dryness and then partitioned between dichloromethane and a saturated aqueous solution of sodium chloride. The layers were separated and the organic phase was washed twice with a saturated aqueous solution of sodium chloride. The organics were concentrated to yield diethyl 2-(2-bromo-4-nitrophenyl)-2-methylmalonate (8.4 g, 99%) as a pale yellow oil which was used without further purification. Retention time 1.86 min.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US08524767B2 |
|---|
| Quelldatensatz | uspto-grants-2013_09 |
|---|
| ORD ID | ord-36d28dae0c694402b63d442f4eef0be0 |
|---|
| Quellennotiz | uspto-grants-2013_09 |
|---|