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Triphenylphosphine → 2-((Trimethylsilyl)ethynyl)nicotinonitrile

HRID 883902
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HRID 883902 반응식
[CH:1]1[CH:6]=[N:5][C:4](Cl)=[C:3]([C:8]#[N:9])[CH:2]=1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[CH3:29][Si:30]([C:33]#[CH:34])([CH3:32])[CH3:31]>C(N(CC)CC)C.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[CH3:29][Si:30]([CH3:32])([CH3:31])[C:33]#[C:34][C:4]1[N:5]=[CH:6][CH:1]=[CH:2][C:3]=1[C:8]#[N:9]
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참가 물질

6

반응물 3

HCID 11776TriphenylphosphineHCID 66111TrimethylsilylacetyleneHCID 810792-Chloronicotinonitrile

생성물 1

HCID 134111132-((Trimethylsilyl)ethynyl)nicotinonitrile수율 75%

시약·촉매·용매 2

HCID 167845palladium(II) acetate촉매HCID 8471Triethylamine
용매

실험 절차

In a suitably sized pressure vessel, commercially available 2-chloro-nictinonitrile (1.5 g, 10.8 mmol) was combined with triphenylphosphine (0.228 g, 8 mole %) and palladium (II) acetate (0.083 g, 3.5 mol %) in triethylamine (20 mL). Nitrogen was bubbled through the resulting suspension at room temperature for five minutes then trimethylsilylacetylene (8.5 mL, 60.1 mmol) was added, the vessel sealed and immersed in an 80° C. oil bath. After 18.5 h the pressure tube was cooled to room temperature and the contents were filtered. The filtrate was concentrated under vacuum and the crude product purified by flash chromatography on silica gel eluting with EtOAc/hexanes to give the title compound (1.62 g, 75%) as a tan solid.

후처리

  1. customNitrogen was bubbled through the resulting suspension at room temperature for five minutes
  2. customthe vessel sealed
  3. customimmersed in an 80° C.
  4. filtrationthe contents were filtered
  5. concentrationThe filtrate was concentrated under vacuum
  6. customthe crude product purified by flash chromatography on silica gel eluting with EtOAc/hexanes

출처 및 근거

ORD 기록
ord-7185a3d099154f9dbf55437c00752c77
출처 데이터셋
uspto-grants-2012_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08236950B2

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