Bromine → 5-Bromo-2-hydroxy-3-methylbenzaldehyde
反応式
[OH:1][C:2]1[C:9]([CH3:10])=[CH:8][CH:7]=[CH:6][C:3]=1[CH:4]=[O:5].[Br:11]Br>C(O)(=O)C.O>[Br:11][C:7]1[CH:8]=[C:9]([CH3:10])[C:2]([OH:1])=[C:3]([CH:6]=1)[CH:4]=[O:5]参加物
5
実験手順
The solution of 2-Hydroxy-3-methylbenzaldehyde (1.0 g, 7.35 mmole) in acetic acid (6 mL) was cooled to 0° C. (ice bath). Bromine (1.36 g, 8.52 mmole) was added dropwise and allowed to stir for 2 hours. The reaction was warmed to room temperature and diluted with water (100 mL) yielding a light orange precipitate. The solid was filtered and washed with water (10 mL). Dried on high vacuum to give a light brown solid (1.4 g, 88.6%). 1H NMR (CDCl3/400 MHz) 11.16 (s, 1H), 9.79 (s, 1H), 7.48 (s, 1H), 7.46 (s, 1H), 2.23 (s, 3H).
後処理
- customyielding a light orange precipitate
- filtrationThe solid was filtered
- washwashed with water (10 mL)
- customDried on high vacuum
出典と根拠
- ORDレコード
- ord-2129189d30cf43e9beacb6550c373296
- 出典データセット
- uspto-grants-2007_08
- 特許番号
- US07259266B2
反応ノート
読み込み中…