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Triphenylphosphine → 2-((Trimethylsilyl)ethynyl)nicotinonitrile

HRID 2197991
ノート
印刷プレビュー

反応式

HRID 2197991 の反応式
[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]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 11776TriphenylphosphineHCID 66111TrimethylsilylacetyleneHCID 810792-Chloronicotinonitrile

生成物 1

HCID 134111132-((Trimethylsilyl)ethynyl)nicotinonitrile収率 75%

試薬・触媒・溶媒 2

HCID 167845palladium(II) acetate触媒HCID 8471Triethylamine
溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-a4ee9cd44c504768a05dd0feac1534d0
出典データセット
uspto-grants-2012_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08338605B2

反応ノート

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