Ethanol → Ethyl 2-fluoro-4-iodobenzoate

HRID 1282312노트

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HRID 1282312 반응식
[F:1][C:2]1[CH:10]=[C:9]([I:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH2:12](O)[CH3:13].S(=O)(=O)(O)O>>[F:1][C:2]1[CH:10]=[C:9]([I:11])[CH:8]=[CH:7][C:3]=1[C:4]([O:6][CH2:12][CH3:13])=[O:5]

참가 물질

4

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온도
90 °C

실험 절차

To a solution of 2.5 g (27.0 mmol) of 2-fluoro-4-iodobenzoic acid (Compound B) in 11 mL (8.6 g, 187.5 mmol) of ethanol was added 0.3 mL of c. sulfuric acid. The reaction mixture was heated to reflux in an oil bath (90° C.) for 1.75 hours, fitted with a short path distillation apparatus, distilled and then allowed to cool to ambient temperature. The reaction mixture was extracted and partitioned between pentane and water and the layers were separated. The aqueous phase was washed with pentane and the organic phases were combined. The combined organic phase was washed sequentially with sat. NaHCO3 (aq.) solution, water and brine, dried over MgSO4, filtered and concentrated in vacuo to a purple oil. Purification by flash chromatography (silica, 10% ethyl acetate in hexane) gave the title compound as an orange oil.

후처리

  1. temperatureThe reaction mixture was heated
  2. customfitted with a short path distillation apparatus
  3. distillationdistilled
  4. temperatureto cool to ambient temperature
  5. extractionThe reaction mixture was extracted
  6. custompartitioned between pentane and water
  7. customthe layers were separated
  8. washThe aqueous phase was washed with pentane
  9. washThe combined organic phase was washed sequentially with sat. NaHCO3 (aq.) solution, water and brine
  10. dry with materialdried over MgSO4
  11. filtrationfiltered
  12. concentrationconcentrated in vacuo to a purple oil
  13. customPurification by flash chromatography (silica, 10% ethyl acetate in hexane)

출처 및 근거

ORD 기록
ord-64d682d8bd5a4b6aaf6e605f6e60de64
출처 데이터셋
uspto-grants-2002_09
특허 번호
US06455701B1

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