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Acetonitrile → 2-Fluoro-5-nitropyridine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| 反応物 | Potassium Fluoride | HCID 522689 | — |
| 触媒 | Tetraphenylphosphonium Bromide | HCID 2724163 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 生成物 | 2-Fluoro-5-nitropyridine | HCID 95264 | — |
反応手順
2-Chloro-5-nitropyridine (100 g, 0.656 mol, Aldrich), KF (84.1 g, 1.448 mol), Ph4PBr (95.3 g, 0.227 mol) and acetonitrile (1.5 L) were combined and heated at reflux until no starting material remained. The volume was reduced to 750 mL, and the mixture was diluted with 2 L of ether, filtered and concentrated. The residue was triturated with hot hexane (5×1 L). The hexane extracts were combined and concentrated to afford 48 g (54%). 1H NMR (CDCl3, 300 MHz) δ7.15 (dd, J=3, 6 Hz, 1H), 8.64 (m, 1H), 9.15 (d, J=1.6 Hz, 1H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05733912 |
| 出典データセット | uspto-grants-1998_03 |
| ORD ID | ord-c3b0e2987bf6463288457f21739f34ea |
| 出典メモ | uspto-grants-1998_03 |