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Hydrogen Bromide → 4-Bromo-3-fluoro-2-hydroxybenzaldehyde

HRID 531107
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HRID 531107 반응식
Br.[Br:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[C:5]([O:11]C)[C:4]=1[F:13]>C(O)(=O)C>[Br:2][C:3]1[CH:10]=[CH:9][C:6]([CH:7]=[O:8])=[C:5]([OH:11])[C:4]=1[F:13]
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참가 물질

4

반응물 2

HCID 260Hydrogen BromideHCID 840385064-Bromo-3-fluoro-2-methoxybenzaldehyde

생성물 1

HCID 978894044-Bromo-3-fluoro-2-hydroxybenzaldehyde수율 70.4%

시약·촉매·용매 1

HCID 176Acetic Acid용매

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온도
120 °C

실험 절차

48% Hydrobromic acid (254 mL) was added to a solution of 4-bromo-3-fluoro-2-methoxybenzaldehyde (52.3 g) in acetic acid (350 mL) at room temperature. The mixture was stirred at 120° C. under nitrogen atmosphere for 16 hours and concentrated in vacuo. The residue was diluted with ethyl acetate and water. The mixture was extracted with ethyl acetate. The organic layer was separated, washed with water and brine, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was triturated with diisopropyl ether and collected by filtration to give the title compound (34.6 g).

후처리

  1. concentrationconcentrated in vacuo
  2. additionThe residue was diluted with ethyl acetate and water
  3. extractionThe mixture was extracted with ethyl acetate
  4. customThe organic layer was separated
  5. washwashed with water and brine
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customThe residue was triturated with diisopropyl ether
  9. filtrationcollected by filtration

출처 및 근거

ORD 기록
ord-e9cf6a8b69c14685bccbcb8f137f21d5
출처 데이터셋
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09353108B2

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