3-Fluoro-2-nitrophenol → 2-amino-3-fluorophenol
反応式
[N+:1]([C:4]1[C:9]([F:10])=[CH:8][CH:7]=[CH:6][C:5]=1[OH:11])([O-])=O>CO.[Pd]>[NH2:1][C:4]1[C:9]([F:10])=[CH:8][CH:7]=[CH:6][C:5]=1[OH:11]参加物
4
実験手順
To a solution of 2-nitro-3-fluorophenol(1 g, 6.4 mmol) in methanol(250 mL) was added 10% Pd/C (1 g). The mixture was flushed with argon, then hydrogen was bubbled through the solution for 10 min. and a hydrogen atmosphere was maintained at balloon pressure overnight. The mixture was filtered through celite and the celite was washed with methanol. The solvent was evaporated and chromatography of the resulting solid on silica gel (5% MeOH/CH2Cl2) gave the desired product(650 mg, 80.2%). 1H NMR (CD3OD): δ 6.41-6.17 (m, 3H).
後処理
- customThe mixture was flushed with argon
- customhydrogen was bubbled through the solution for 10 min.
- temperaturea hydrogen atmosphere was maintained at balloon pressure overnight
- filtrationThe mixture was filtered through celite
- washthe celite was washed with methanol
- customThe solvent was evaporated
出典と根拠
- ORDレコード
- ord-bbce35a140d04ce3a42a7119beb11645
- 出典データセット
- uspto-grants-2001_01
- 特許番号
- US06180675B2
反応ノート
読み込み中…