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Pyridine → 5-Chloro-3-phenyl-1,2,4-oxadiazole

HRID 1195798
ノート
印刷プレビュー

反応式

HRID 1195798 の反応式
P(Cl)(Cl)([Cl:3])=O.[C:6]1([C:12]2[N:16]=[C:15](O)[O:14][N:13]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.N1C=CC=CC=1>>[C:6]1([C:12]2[N:16]=[C:15]([Cl:3])[O:14][N:13]=2)[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 1049PyridineHCID 24813Phosphorus oxychlorideHCID 178517464HCID 178517464、化合物

生成物 1

HCID 127284435-Chloro-3-phenyl-1,2,4-oxadiazole

実験手順

To 53 g of phosphorus oxychloride were added 12.6 g (18 mmol) of 3-phenyl-1,2,4-oxadiazol-5-ol, followed by the further addition of 2.8 g (35 mmol of pyridine. The resultant mixture was heated under stirring for 8 hours. The reaction mixture was allowed to cool down to room temperature and then transferred into 500 ml of ice water. The resultant liquid mixture was extracted with ether. The extract was washed successively with water, a 5% aqueous solution of sodium hydroxide and water. The organic layer was dried and the solvent was distilled off. When the residue was left over under cooling, the title compound was obtained as pale brown crystals.

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
extraction
The resultant liquid mixture was extracted with ether
  • washThe extract was washed successively with water
  • customThe organic layer was dried
  • distillationthe solvent was distilled off
  • waitWhen the residue was left over
  • temperatureunder cooling
  • 出典と根拠

    ORDレコード
    ord-4370dca4fe0d4759bff0dd6d450dc528
    出典データセット
    uspto-grants-1992_05
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US05112841

    反応ノート

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