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Acetic Acid → (3-Bromo-2,5-dimethoxy-phenyl)-acetic acid

HRID 1794494
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HRID 1794494 반응식
[Br:1][C:2]1[C:3]([O:13][CH3:14])=[C:4](CC#N)[CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1.[CH3:15][C:16]([OH:18])=[O:17]>O.OS(O)(=O)=O>[Br:1][C:2]1[C:3]([O:13][CH3:14])=[C:4]([CH2:15][C:16]([OH:18])=[O:17])[CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1
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참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 10149238(3-Bromo-2,5-dimethoxy-phenyl)-acetonitrile

생성물 1

HCID 10125382(3-Bromo-2,5-dimethoxy-phenyl)-acetic acid수율 55%

시약·촉매·용매 2

HCID 962Water용매2회HCID 1118Sulfuric Acid용매

실험 절차

A solution of (3-Bromo-2,5-dimethoxy-phenyl)-acetonitrile 54 (5.2 g, 20.4 mmol) in water (10 ml), conc H2SO4 (10 ml), and AcOH (30 ml) was heated to 100° C. After 3 hr the reaction was cooled; and poured into water. The aqueous layer was extracted with EtOAc which was then dried over MgSO4, filtered and concentrated. The product was purified by column chromatography on silica gel (50% EtOAc/Hex) to give a solid (2.8 g, 55%): Mp=62–65° C.; 1H NMR (DMSO-d6) δ 12.45 (br s, 1 H), 7.09 (d, 1 H, J=2.9 Hz), 6.87 (d, 1 H, J=3.0 Hz), 3.72 (s, 3 H), 3.66 (s, 3 H), 3.59 (s, 2 H); MS 273/27 (M−H)−.

후처리

  1. temperatureAfter 3 hr the reaction was cooled
  2. extractionThe aqueous layer was extracted with EtOAc which
  3. dry with materialwas then dried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe product was purified by column chromatography on silica gel (50% EtOAc/Hex)

출처 및 근거

ORD 기록
ord-9151dc9db81e46da9cc46b27f8c3da9d
출처 데이터셋
uspto-grants-2006_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07022733B2

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