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Nicotinic Acid → N-Methoxy-N-methylnicotinamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Nicotinic Acid | HCID 938 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | N,O-Dimethylhydroxylamine | HCID 14232 | — |
| 反応物 | Thionyl Chloride | HCID 24386 | — |
| 生成物 | N-Methoxy-N-methylnicotinamide | HCID 10558996 | — |
反応手順
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)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09242963B2 |
| 出典データセット | uspto-grants-2016_01 |
| ORD ID | ord-cdf6e6329b7044669a3248a1d08e0744 |
| 出典メモ | uspto-grants-2016_01 |