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Water → 6-Fluoro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile

HRID 392369
ノート
印刷プレビュー

反応式

HRID 392369 の反応式
Cl[C:2]1[N:7]=[C:6]([C:8]#[N:9])[C:5]([S:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[N:4][CH:3]=1.[F-:17].[K+].C(OCC)(=O)C.O>CS(C)=O.[Br-].C([N+](CCCC)(CCCC)CCCC)CCC>[F:17][C:2]1[N:7]=[C:6]([C:8]#[N:9])[C:5]([S:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[N:4][CH:3]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 962WaterHCID 8857Ethyl AcetateHCID 522689Potassium FluorideHCID 226628046-Chloro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile

生成物 1

HCID 226628496-Fluoro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile収率 53.6%

試薬・触媒・溶媒 2

HCID 74236
Tetrabutylammonium Bromide
触媒
HCID 679Dimethyl Sulfoxide溶媒

反応条件

温度
55 °C

実験手順

In 3.6 mL of dimethyl sulfoxide was dissolved 0.20 g of 6-chloro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile. After adding 0.42 g of potassium fluoride and 0.16 g of tetra-n-butylammonium bromide successively, the mixture thus obtained was stirred at 50-60° C. for 2.5 hours. The reaction mixture was poured into a mixture of 20 mL of ethyl acetate and 20 mL of water, and the organic layer was separated. The organic layer was washed successively with water and saturated aqueous solution of sodium chloride and dried on anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue thus obtained was purified by silica gel column chromatography [eluent: toluene:n-hexane=1:2] to obtain 0.10 g of 6-fluoro-3-(phenylsulfanyl)-2-pyrazinecarbonitrile as a light yellow-colored oily product.

後処理

  1. customthe mixture thus obtained
  2. customthe organic layer was separated
  3. washThe organic layer was washed successively with water and saturated aqueous solution of sodium chloride
  4. dry with materialdried on anhydrous magnesium sulfate
  5. customthe solvent was removed under reduced pressure
  6. customThe residue thus obtained
  7. customwas purified by silica gel column chromatography [eluent: toluene:n-hexane=1:2]

出典と根拠

ORDレコード
ord-4c2f1268c881457ba9eac2091be0501b
出典データセット
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06800629B2

反応ノート

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