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Water → 6-Fluoro-2-hydroxy-3-methoxybenzaldehyde

HRID 751554
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HRID 751554 반응식
B(Cl)(Cl)Cl.[F:5][C:6]1[C:11]([CH:12]=[O:13])=[C:10]([O:14]C)[C:9]([O:16][CH3:17])=[CH:8][CH:7]=1.O>ClCCl>[F:5][C:6]1[C:11]([CH:12]=[O:13])=[C:10]([OH:14])[C:9]([O:16][CH3:17])=[CH:8][CH:7]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 25135Boron TrichlorideHCID 107261486-Fluoro-2,3-dimethoxybenzaldehyde

생성물 1

HCID 224828186-Fluoro-2-hydroxy-3-methoxybenzaldehyde수율 95.1%

시약·촉매·용매 1

HCID 6344Dichloromethane용매2회

실험 절차

1M boron trichloride in dichloromethane (25 ml; 25 mmol) was added to a solution of 6-fluoro-2,3-dimethoxy-benzaldehyde [Cantrell, Amanda S.; Engelhardt, Per; Hoegberg, Marita; Jaskunas, S. Richard; Johansson, Nils Gunnar; et al.; J.Med.Chem.; 39; 21; 1996; 4261-4274] (4.26 g; 23 mmol) in dichloromethane (30 ml) keeping the reaction temperature at −70 C. The reaction mixture stirred at room temperature overnight and hydrolyzed with water. The organic phase was separated, washed with water and evaporated in vacuo. The residue was chromatographed (silica gel, EA:Hex, 5:1) to give 3.72 g (94%) of 6-fluoro-2-hydroxy-3-methoxy-benzaldehyde as yellow crystals.

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후처리

  1. customThe organic phase was separated
  2. washwashed with water
  3. customevaporated in vacuo
  4. customThe residue was chromatographed (silica gel, EA:Hex, 5:1)

출처 및 근거

ORD 기록
ord-a19a8a734c5445749e09d85bfc25132d
출처 데이터셋
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07405310B2

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