Boron tribromide → 4-Fluoro-2,3-dihydroxybenzaldehyde
反応式
C[O:2][C:3]1[C:10]([O:11]C)=[C:9]([F:13])[CH:8]=[CH:7][C:4]=1[CH:5]=[O:6].B(Br)(Br)Br>ClCCl>[F:13][C:9]1[CH:8]=[CH:7][C:4]([CH:5]=[O:6])=[C:3]([OH:2])[C:10]=1[OH:11]参加物
反応条件
- 温度
- -78 °C
実験手順
To a solution at −78° C. of 2,3-dimethoxy-4-fluorobenzaldehyde (7.0 g, 38.0 mmol) in dry dichloromethane (150 mL) was added dropwise BBr3 (23.8 g, 95.0 mmol) in dichloromethane (30 mL). Reaction mixture was allowed to attain room temperature and stirred for 18 h. Then reaction mixture was cooled to −78° C., and quenched with a mixture of methanol (10 mL) and water (50 mL) and stirred at room temperature for 30 min. Precipitated solid was separated by filtration and washed with cold dichloromethane. Dichloromethane layer was concentrated to yield the title compound as a solid (5.2 g, 88%). 1H NMR (400 MHz, CHLOROFORM-d) δ ppm: 11.38 (s, 1H), 9.84 (s, 1H), 7.15 (dd, J=8.6, 5.5 Hz, 1H), 6.81 (t, J=9.4 Hz, 1H), 5.47 (s, 1H); MS (ESI) m/z=155 (M−1, negative).
後処理
- customReaction mixture
- customto attain room temperature
- customThen reaction mixture
- customquenched with a mixture of methanol (10 mL) and water (50 mL)
- stirringstirred at room temperature for 30 min
- customPrecipitated solid
- customwas separated by filtration
- washwashed with cold dichloromethane
- concentrationDichloromethane layer was concentrated
出典と根拠
- ORDレコード
- ord-371f926d4f8d45c1a3a58391eead2d27
- 出典データセット
- uspto-grants-2014_04
- 特許番号
- US08703742B2
反応ノート
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