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Phosphorus oxychloride → 4-Chloro-6-(4-bromophenyl)thieno[3,2-c]pyridine

HRID 1814496
ノート
印刷プレビュー

反応式

HRID 1814496 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:13][C:12](=O)[C:11]3[CH:15]=[CH:16][S:17][C:10]=3[CH:9]=2)=[CH:4][CH:3]=1.P(Cl)(Cl)([Cl:20])=O>>[Cl:20][C:12]1[C:11]2[CH:15]=[CH:16][S:17][C:10]=2[CH:9]=[C:8]([C:5]2[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][CH:4]=2)[N:13]=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

3

反応物 2

HCID 24813Phosphorus oxychlorideHCID 225024536-(4-bromophenyl)-5H-thieno[3,2-c]pyridin-4-one

生成物 1

HCID 225035574-Chloro-6-(4-bromophenyl)thieno[3,2-c]pyridine

反応条件

温度
100 °C

実験手順

6-(4-Bromophenyl)-5H-thieno[3,2-c]pyridin-4-one (4.87 g) was added to phosphorus oxychloride (30 ml), and the resulting mixture was heated at 100° C. for 3 hr. The reaction solution was evaporated, and to the resulting residue were added ethyl acetate and water. The organic layer was washed with water, an aqueous solution of saturated sodium bicarbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, to give 4-chloro-6-(4-bromophenyl)thieno[3,2-c]pyridine.

後処理

  1. custom
The reaction solution was evaporated
  • additionto the resulting residue were added ethyl acetate and water
  • washThe organic layer was washed with water
  • dry with materialan aqueous solution of saturated sodium bicarbonate and brine, and dried over magnesium sulfate
  • customThe solvent was evaporated
  • 出典と根拠

    ORDレコード
    ord-495c886d53cc49c48b2a090a71ac7bf2
    出典データセット
    uspto-grants-2005_04
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06875761B2

    反応ノート

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    このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート