Boron tribromide → 4-Fluoro-2,3-dihydroxybenzaldehyde

HRID 2368013ノート

反応式

HRID 2368013 の反応式
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

4

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

  1. customReaction mixture
  2. customto attain room temperature
  3. customThen reaction mixture
  4. customquenched with a mixture of methanol (10 mL) and water (50 mL)
  5. stirringstirred at room temperature for 30 min
  6. customPrecipitated solid
  7. customwas separated by filtration
  8. washwashed with cold dichloromethane
  9. 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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