Triethylamine → 2-Cyano-3-fluoropyridine
反応式
[F:1][C:2]1[CH:3]=[N+:4]([O-])[CH:5]=[CH:6][CH:7]=1.C[Si]([C:13]#[N:14])(C)C.C(N(CC)CC)C>C(#N)C>[C:13]([C:3]1[C:2]([F:1])=[CH:7][CH:6]=[CH:5][N:4]=1)#[N:14]参加物
5
実験手順
3-Fluoropyridine-1-oxide (10.0g, 88.4 mmol), trimethylsilylcyanide (26.32g, 265.3 mmol), and triethylamine (17.89g, 177 mmol) were reacted in 90 mL of acetonitrile utilizing the procedure described in example 762B. Purification of the crude by silica gel chomatography using CH2Cl2 as eluent gives compound 771B (7.5g, 70%) as a light yellow solid.
後処理
- customPurification of the crude by silica gel chomatography
出典と根拠
- ORDレコード
- ord-08b764105c2d4d27b5ea0492d2a71faa
- 出典データセット
- uspto-grants-2006_11
- 特許番号
- US07141578B2
反応ノート
読み込み中…