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Acetone → 2-(5-Bromo-3-fluoropyridin-2-yl)propan-2-ol

HRID 589191
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HRID 589191 반응식
Br[C:2]1[C:7]([F:8])=[CH:6][C:5]([Br:9])=[CH:4][N:3]=1.C([Li])CCC.[CH3:15][C:16]([CH3:18])=[O:17]>C1(C)C=CC=CC=1>[Br:9][C:5]1[CH:6]=[C:7]([F:8])[C:2]([C:16]([OH:17])([CH3:18])[CH3:15])=[N:3][CH:4]=1
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참가 물질

5

반응물 3

HCID 180AcetoneHCID 224128322,5-Dibromo-3-fluoropyridineHCID 178418339Butyllithium

생성물 1

HCID 672950462-(5-Bromo-3-fluoropyridin-2-yl)propan-2-ol

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
-78 °C

실험 절차

To 2,5-dibromo-3-fluoropyridine in toluene at −78° C. was added n-butyllithium drop wise. The resulting solution was stirred at −78° C. for 1.5 hours. Then at −78° C., added acetone drop wise to the reaction mixture and continue to stir reaction at −78° C. for 2 hours at which point LC-MS and TLC indicated the reaction was complete. The reaction was warmed to 0° C. and quenched with saturated ammonium chloride solution (aq.) and then diluted with water (50 mL) and extracted with ethyl acetate (2×100 mL). The organic layer was dried (Na2SO4) and concentrated in vacuo to afford crude product. Gradient column chromatography on silica eluting with 0 to 30% EtOAc/hexanes gave the desired product (1.04 g).

후처리

  1. stirringto stir
  2. customreaction at −78° C. for 2 hours at which point LC-MS and TLC
  3. temperatureThe reaction was warmed to 0° C.
  4. customquenched with saturated ammonium chloride solution (aq.)
  5. additiondiluted with water (50 mL)
  6. extractionextracted with ethyl acetate (2×100 mL)
  7. dry with materialThe organic layer was dried (Na2SO4)
  8. concentrationconcentrated in vacuo
  9. customto afford crude product

출처 및 근거

ORD 기록
ord-5732a6fe1f844aeea5063cee2d63e99f
출처 데이터셋
uspto-grants-2016_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09227971B2

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