反応式
[Br:1][C:2]1[CH:3]=[C:4]([CH2:11][OH:12])[CH:5]=[C:6]([N+:8]([O-])=O)[CH:7]=1>CO.[Pt](=O)=O>[NH2:8][C:6]1[CH:5]=[C:4]([CH2:11][OH:12])[CH:3]=[C:2]([Br:1])[CH:7]=1参加物
4
実験手順
(3-Bromo-5-nitrophenyl)methanol (3.9 g, 16.8 mmol) in methanol (35 mL) was flushed with nitrogen, and treated with platinum (IV) oxide (390 mg). The flask was flushed with hydrogen and allowed to stir under an atmosphere of hydrogen for 1 h. The reaction was flushed with nitrogen, filtered through celite, and concentrated to afford 3.1 g (94%). 1H-NMR (CDCl3, 300 MHz) δ 6.95 (s, 1H), 6.80 (s, 1H), 6.79 (s, 1H), 4.61 (s, 2H). Mass spec.: 203.96 (MH)+.
後処理
- customThe flask was flushed with hydrogen
- customThe reaction was flushed with nitrogen
- filtrationfiltered through celite
- concentrationconcentrated
- customto afford 3.1 g (94%)
出典と根拠
- ORDレコード
- ord-e4f63e5b3b20495b971be59e1fb5bc9b
- 出典データセット
- uspto-grants-2013_02
- 特許番号
- US08383821B2
関連ノート
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