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Ethanol → Ethyl 2,5-dibromoisonicotinate

HRID 2047587
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HRID 2047587 반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:8]([Br:11])=[CH:9][N:10]=1)[C:5]([OH:7])=[O:6].S(=O)(=O)(O)O.[CH2:17](O)[CH3:18]>>[Br:1][C:2]1[CH:3]=[C:4]([C:8]([Br:11])=[CH:9][N:10]=1)[C:5]([O:7][CH2:17][CH3:18])=[O:6]
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참가 물질

4

반응물 3

HCID 702Ethanol2회HCID 1118Sulfuric AcidHCID 263436962,5-Dibromoisonicotinic acid

생성물 1

HCID 46311329Ethyl 2,5-dibromoisonicotinate

실험 절차

A solution of 2,5-dibromoisonicotinic acid (1-1, 5 g, 17.80 mmol) and sulfuric acid (1.23 mL, 23.1 mmol) in ethanol (100 mL) was heated to reflux overnight. After reducing the volume of ethanol by rotary evaporation to approximately ¼ of it's original volume, the crude reaction mixture was partitioned between 2M sodium carbonate solution and EtOAc, separating layers and washing the organic layer with saturated sodium bicarbonate solution and brine. This solution was dried over anhydrous sodium sulfate, filtered and concentrated. The residue was purified by normal phase column chromatography (0 to 50% EtOAc in hexanes) to afford the product (1-2) as a dark oil. ESI+MS [M]+C8H7Br2NO2=308.0.

후처리

  1. temperatureto reflux overnight
  2. customby rotary evaporation to approximately ¼ of it's original volume
  3. customthe crude reaction mixture
  4. customwas partitioned between 2M sodium carbonate solution and EtOAc
  5. customseparating layers
  6. washwashing the organic layer with saturated sodium bicarbonate solution and brine
  7. dry with materialThis solution was dried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe residue was purified by normal phase column chromatography (0 to 50% EtOAc in hexanes)

출처 및 근거

ORD 기록
ord-179c8600570a4667b0afd296c402cf80
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08592457B2

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