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Bromine → Methyl 5-bromo-2-fluoro-4-hydroxybenzoate

HRID 1662426
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HRID 1662426 반응식
[F:1][C:2]1[CH:11]=[C:10]([OH:12])[CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].[Br:13]Br>C(O)(=O)C>[Br:13][C:9]1[C:10]([OH:12])=[CH:11][C:2]([F:1])=[C:3]([CH:8]=1)[C:4]([O:6][CH3:7])=[O:5]
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참가 물질

4

반응물 2

HCID 24408BromineHCID 22463192Methyl 2-fluoro-4-hydroxybenzoate

생성물 1

HCID 57467602Methyl 5-bromo-2-fluoro-4-hydroxybenzoate수율 71.5%

시약·촉매·용매 1

HCID 176Acetic Acid용매2회

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온도
45 °C

실험 절차

To a solution of 66.43A (2.03 g, 11.9 mmol) in acetic acid (65 mL) was added a pre-mixed solution of bromine (0.67 mL, 13.1 mmol) in acetic acid (10 mL). The mixture was stirred at 45° C. and monitored with TLC and LC-MS. After 18 hours, the reaction mixture was concentrated under reduced pressure. Brine was added to the residue, and the mixture was extracted three times with EtOAc. The combined organic layers were dried over anhydrous magnesium sulfate, filtered and concentrated to provide 66.43B as a white solid (2.12 g, 71% yield). 1H NMR (400 MHz, CDCl3) δ ppm 8.13 (1H, d, J=7.4 Hz), 6.82 (1H, d, J=11.3 Hz), 6.04 (1H, s), 3.92 (3H, s).

후처리

  1. concentrationthe reaction mixture was concentrated under reduced pressure
  2. additionBrine was added to the residue
  3. extractionthe mixture was extracted three times with EtOAc
  4. dry with materialThe combined organic layers were dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationconcentrated

출처 및 근거

ORD 기록
ord-4943c58f006b456fb1196bd72bbd9732
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08030354B2

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