Carbon Dioxide → 5-Bromo-2,3,4-trifluorobenzoic acid

HRID 558241

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HRID 558241 반응식
N(C(C)C)C(C)C.[Li]CCCC.[Br:13][C:14]1[CH:19]=[CH:18][C:17]([F:20])=[C:16]([F:21])[C:15]=1[F:22].[C:23](=[O:25])=[O:24]>C1COCC1>[Br:13][C:14]1[C:15]([F:22])=[C:16]([F:21])[C:17]([F:20])=[C:18]([CH:19]=1)[C:23]([OH:25])=[O:24]

참가 물질

6

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온도
0 °C

실험 절차

To a solution of iPr2NH (56.8 mmol, 8 ml) in THF (50 ml) at −78° C. was added dropwise a solution of nBuLi (1.6M in hexane, 56.8 ml, 35.5 mmol). The dry ice bath was removed and the mixture was stirred at 0° C. for ˜15 min. The mixture is transferred via cannula to a solution of 1-bromo-2,3,4-trifluorobenzene (47.4 mmol, 10 g) in THF (50 ml) cooled at −78° C. The orange solution was stirred at −78° C. for 1 h, then transferred, via cannula, to freshly grinded dry CO2. The reaction was warmed up to room temperature and stirred overnight. The reaction mixture was cooled at 0° C., quenched with 10% HCl (300 ml), extracted with ether (100 ml×3), dry over MgSO4 and concentrated under reduced pressure to obtain (10.6 g, 88%) of the title compound.

후처리

  1. customThe dry ice bath was removed
  2. temperaturecooled at −78° C
  3. stirringThe orange solution was stirred at −78° C. for 1 h
  4. temperatureThe reaction was warmed up to room temperature
  5. stirringstirred overnight
  6. temperatureThe reaction mixture was cooled at 0° C.
  7. customquenched with 10% HCl (300 ml)
  8. extractionextracted with ether (100 ml×3)
  9. dry with materialdry over MgSO4
  10. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-d6a4fcbb976440079bb1606a45ae0388
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08063049B2

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