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

HRID 2368013노트

반응식

HRID 2368013 반응식
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]

참가 물질

4

반응 조건

온도
-78 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-371f926d4f8d45c1a3a58391eead2d27
출처 데이터셋
uspto-grants-2014_04
특허 번호
US08703742B2

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