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(Trifluoromethyl)trimethylsilane → 1-(5-Bromopyridin-2-yl)-2,2,2-trifluoroethan-1-ol

HRID 1053946
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HRID 1053946 반응식
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]=[O:9])=[N:6][CH:7]=1.[F:10][C:11]([Si](C)(C)C)([F:13])[F:12].CCCC[N+](CCCC)(CCCC)CCCC.[F-]>C1COCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]([OH:9])[C:11]([F:13])([F:12])[F:10])=[N:6][CH:7]=1
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참가 물질

5

반응물 3

HCID 552549(Trifluoromethyl)trimethylsilaneHCID 2724141Tetrabutylammonium FluorideHCID 98775625-Bromopyridine-2-carbaldehyde

생성물 1

HCID 672947601-(5-Bromopyridin-2-yl)-2,2,2-trifluoroethan-1-ol

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

5-Bromopicolinaldehyde (500 mg, 2.70 mmol) was dissolved in THF (9.0 mL) and the flask was then sealed with a septum, flushed with argon, and cooled to 0° C. (Trifluoromethyl)trimethylsilane (0.44 mL, 3.0 mmol) was then added followed by TBAF (2.7 mL, 2.7 mmol, 1M in THF). The resulting mixture was allowed to warm to ambient temperature and was stirred for 2 hours. The reaction was then quenched with water and extracted with DCM (2×). The combined organic extracts were washed with brine, dried over anhydrous MgSO4, and concentrated in vacuo. The residue was purified by MPLC on silica gel (using a gradient elution of 10-20% EtOAc/hexanes) to afford the title compound. LRMS (ESI) calc'd for C8H6BrF3O [M+H]+: 256. Found: 256.

후처리

  1. customthe flask was then sealed with a septum
  2. customflushed with argon
  3. additionwas then added
  4. customThe reaction was then quenched with water
  5. extractionextracted with DCM (2×)
  6. washThe combined organic extracts were washed with brine
  7. dry with materialdried over anhydrous MgSO4
  8. concentrationconcentrated in vacuo
  9. customThe residue was purified by MPLC on silica gel (
  10. washa gradient elution of 10-20% EtOAc/hexanes)

출처 및 근거

ORD 기록
ord-99f8308bcd8a4a9fa6b713fbb3d3a5f3
출처 데이터셋
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09394282B2

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