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Dimethyl Sulfate → 3-Fluoro-2-methoxybenzaldehyde

HRID 1822946
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HRID 1822946 반응식
[F:1][C:2]1[C:3]([OH:10])=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6].[C:11](=O)([O-])[O-].[K+].[K+].S(OC)(OC)(=O)=O>CC(C)=O>[F:1][C:2]1[C:3]([O:10][CH3:11])=[C:4]([CH:7]=[CH:8][CH:9]=1)[CH:5]=[O:6]
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참가 물질

5

반응물 3

HCID 6497Dimethyl SulfateHCID 11430Potassium CarbonateHCID 5877883-Fluorosalicylaldehyde

생성물 1

HCID 125722773-Fluoro-2-methoxybenzaldehyde수율 100%

시약·촉매·용매 1

HCID 180Acetone용매

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온도
60 °C

실험 절차

To a suspension of 3-fluoro-2-hydroxybenzaldehyde (5.328 g, 38.02 mmol) and potassium carbonate (7.88 g, 57.03 mmol) in acetone (60 mL) was added dimethyl sulphate (3.96 mL, 41.83 mmol). The resulting suspension was stirred at 60° C. for 2 h before being allowed to cool and then concentrated in vacuo. The residue was dissolved in dichloromethane (100 mL) and water (50 mL). The organic phase was washed with saturated sodium bicarbonate (50 mL) with the resulting organic phase being dried (MgSO4) and the solvent evaporated in vacuo to give a pale yellow oil (6.262 g, 38.02 mmol, 100%). δH (300 MHz, CDCl3) 10.40 (1H, s, CHO), 7.60 (1H, d, Ar), 7.30 (1H), m, Ar), 7.10 (1H, m, Ar), 4.10 (3H, s, OCH3).

후처리

  1. temperatureto cool
  2. concentrationconcentrated in vacuo
  3. dissolutionThe residue was dissolved in dichloromethane (100 mL)
  4. washThe organic phase was washed with saturated sodium bicarbonate (50 mL) with the resulting organic phase
  5. dry with materialbeing dried (MgSO4)
  6. customthe solvent evaporated in vacuo

출처 및 근거

ORD 기록
ord-dea8fbd647054bb8bf75d4a2a50da8c9
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07037932B2

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