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Trimethylsilyl cyanide → 2-(3-Chloro-2-fluorophenyl)acetonitrile

HRID 2277577
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HRID 2277577 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH2:8]Br)[C:3]=1[F:10].C[Si]([C:15]#[N:16])(C)C.CCCC[N+](CCCC)(CCCC)CCCC.[F-]>CC#N>[Cl:1][C:2]1[C:3]([F:10])=[C:4]([CH2:8][C:15]#[N:16])[CH:5]=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 82115Trimethylsilyl cyanideHCID 5228271-(Bromomethyl)-3-chloro-2-fluorobenzeneHCID 2724141Tetrabutylammonium Fluoride

생성물 1

HCID 27737242-(3-Chloro-2-fluorophenyl)acetonitrile수율 88%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

To a solution of 1-chloro-3-bromomethyl-2-fluoro-benzene (2.22 g, 10 mmol) in CH3CN (30 mL) was added trimethylsilyl cyanide (1.5 mL) and TBAF (1M in THF, 12 mmol, 12 mL). The resulting reaction mixture was heated at reflux temperature for 30 min. After cooling to room temperature, the volatiles were evaporated under reduced pressure. The residue was partitioned between EtOAc and water. The organic layer was then washed with brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo. The crude product was purified by flash column chromatography to give the title compound (1.48 g, 88%). MS: 170.1 (M+H)+.

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후처리

  1. customThe resulting reaction mixture
  2. temperaturewas heated
  3. temperatureat reflux temperature for 30 min
  4. customthe volatiles were evaporated under reduced pressure
  5. customThe residue was partitioned between EtOAc and water
  6. washThe organic layer was then washed with brine
  7. customdried over anhy
  8. filtrationNa2SO4, filtered
  9. concentrationconcentrated in vacuo
  10. customThe crude product was purified by flash column chromatography

출처 및 근거

ORD 기록
ord-e99838d0abde499188cad416617c0b87
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133158B2

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