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Carbon Dioxide → 6-Bromo-2,3-difluorobenzoic acid

HRID 497989
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HRID 497989 반응식
C([Li])CCC.CCCCCC.CC1(C)CCCC(C)(C)N1.[Br:22][C:23]1[CH:28]=[CH:27][C:26]([F:29])=[C:25]([F:30])[CH:24]=1.[C:31](=[O:33])=[O:32]>O1CCCC1>[Br:22][C:23]1[C:24]([C:31]([OH:33])=[O:32])=[C:25]([F:30])[C:26]([F:29])=[CH:27][CH:28]=1
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참가 물질

7

반응물 5

HCID 280Carbon DioxideHCID 8058HexaneHCID 130352,2,6,6-TetramethylpiperidineHCID 676754-Bromo-1,2-difluorobenzeneHCID 178418339Butyllithium

생성물 1

HCID 223202686-Bromo-2,3-difluorobenzoic acid수율 57%

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

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온도
-78 °C

실험 절차

A solution of 1.6M butyllithium in hexane (60 mL, 96 mmol) was diluted with tetrahydrofuran (180 mL) under an argon atmosphere, and cooled to −78° C. To the solution, were added dropwise 2,2,6,6-tetramethylpiperidine (16.2 g, 116 mmol) and subsequently 4-bromo-1,2-difluorobenzene (15.4 g, 80 mmol), and the mixture was stirred at the same temperature for 2 hours. The solution was carefully poured onto crushed dry ice, and the mixture was allowed to warm to room temperature. The solution was concentrated under reduced pressure, and the residue was poured into water. After the solution was washed with diethylether, the aqueous layer was made acidic by the addition of 6N hydrochloric acid, and organic matter was extracted with dichloromethane. The extract was washed with saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give the title compound (10.8 g, 57% yield).

후처리

  1. additionThe solution was carefully poured
  2. temperatureto warm to room temperature
  3. concentrationThe solution was concentrated under reduced pressure
  4. additionthe residue was poured into water
  5. washAfter the solution was washed with diethylether
  6. additionthe aqueous layer was made acidic by the addition of 6N hydrochloric acid, and organic matter
  7. extractionwas extracted with dichloromethane
  8. washThe extract was washed with saturated brine
  9. dry with materialdried over anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-f2347a8cfb674342bc9bcef92b938f7e
출처 데이터셋
uspto-grants-2005_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06949648B2

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