HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Water → 4-bromo-3-methyl-N-(trimethylsilylmethyl)benzamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Water | HCID 962 | — |
| Edukt | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Edukt | 4-Bromo-3-methylbenzoic acid | HCID 82131 | — |
| Edukt | 1-(Trimethylsilyl)methylamine | HCID 87488 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 4-bromo-3-methyl-N-(trimethylsilylmethyl)benzamide | HCID 66836469 | 94% |
Reaktionsschritte
To a suspension of 4-bromo-3-methylbenzoic acid (25 g) and 4-(dimethylamino)pyridine (“DMAP”, 2.1 g) in CH2Cl2 (320 mL) was added N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide (“EDC”, 22.4 g) portionwise. Then, (aminomethyl)trimethylsilane (8.6 mL) was added, while cooling to keep the internal temperature below 20° C. The reaction was stirred at room temperature overnight. Water was added under vigorous stirring, and the layers were separated. The aqueous layer was extracted twice with CH2Cl2, and the combined organic phase dried (Na2SO4), and filtered over silica gel using CH2Cl2 and methyl tert-butyl ether (MTBE) to afford the title compound (32.8 g, 94%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08653000B2 |
| Quelldatensatz | uspto-grants-2014_02 |
| ORD ID | ord-84bff735b8e84773b38a246cec69f299 |
| Quellennotiz | uspto-grants-2014_02 |