HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Nicotinic Acid → N-Methoxy-N-methylnicotinamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Nicotinic Acid | HCID 938 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | N,O-Dimethylhydroxylamine | HCID 14232 | — |
| Edukt | Thionyl Chloride | HCID 24386 | — |
| Produkt | N-Methoxy-N-methylnicotinamide | HCID 10558996 | — |
Reaktionsschritte
A flask is charged with nicotinic acid (5.0 g, 40.6 mmol). Thionyl chloride (30.0 mL) is added and the reaction is refluxed for 1 h. It is then cooled to room temperature and concentrated in vacuo. The residue is dissolved in anhydrous dichloromethane (30 mL) and O,N-dimethyl-hydroxylamine (4.35 g, 44.0 mmol) is added, followed by addition of triethylamine (14.15 g, 100.0 mmol). The reaction mixture is stirred at room temperature for 1.5 h. It is then washed with water and the aqueous phase is extracted with dichloromethane. The combined organic layer is dried over sodium sulfate and concentrated in vacuo to afford N-methyl-N-methoxy-nicotinamide as a brown oil. MS (ESI) m/z 167.0 (M+H)+.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US09242963B2 |
| Quelldatensatz | uspto-grants-2016_01 |
| ORD ID | ord-cdf6e6329b7044669a3248a1d08e0744 |
| Quellennotiz | uspto-grants-2016_01 |