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Acetone → 2-(4-Methyl-3-trifluoromethyl-phenyl)-propan-2-ol

HRID 2384828
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HRID 2384828 반응식
Br[C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[C:4]([C:9]([F:12])([F:11])[F:10])[CH:3]=1.[Li]CCCC.[CH3:18][C:19]([CH3:21])=[O:20]>C1COCC1>[CH3:8][C:5]1[CH:6]=[CH:7][C:2]([C:19]([OH:20])([CH3:21])[CH3:18])=[CH:3][C:4]=1[C:9]([F:12])([F:11])[F:10]
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참가 물질

5

반응물 3

HCID 180AcetoneHCID 27756354-Methyl-3-(trifluoromethyl)bromobenzeneHCID 178418339Butyllithium

생성물 1

HCID 672412752-(4-Methyl-3-trifluoromethyl-phenyl)-propan-2-ol수율 86%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
-78 °C

실험 절차

To a solution of 4-Bromo-1-methyl-2-trifluoromethyl-benzene (3.4 g, 14.2 mmol) in THF was added n-BuLi at −78° C. After the reaction mixture was stirred at −78° C. for 30 minutes, dry acetone was slowly added. The resulting content was maintained at −78° C. for 3 hours and slowly warmed up to RT overnight. The reaction mixture was then partitioned between ethyl acetate and water. The ethyl acetate layer was then washed with brine, dried over Na2SO4, filtered, and the solvent evaporated in vacuo to yield a crude oil. The crude solid was purified via flash chromatography (15% EtOAc in n-hexane) yielded the title compound as an oil (2.7 g, 86%).

후처리

  1. temperatureThe resulting content was maintained at −78° C. for 3 hours
  2. temperatureslowly warmed up to RT overnight
  3. customThe reaction mixture was then partitioned between ethyl acetate and water
  4. washThe ethyl acetate layer was then washed with brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. customthe solvent evaporated in vacuo
  8. customto yield a crude oil
  9. customThe crude solid was purified via flash chromatography (15% EtOAc in n-hexane)

출처 및 근거

ORD 기록
ord-22ce048f55134029a8a65dad256fac35
출처 데이터셋
uspto-grants-2012_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08263781B2

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