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Phosphorus oxychloride → 3-Chloro-5-(trifluoromethyl)pyridazine

HRID 2046391
ノート
印刷プレビュー

反応式

HRID 2046391 の反応式
[F:1][C:2]([F:11])([F:10])[C:3]1[CH:8]=[N:7][NH:6][C:5](=O)[CH:4]=1.O=P(Cl)(Cl)[Cl:14]>O1CCOCC1>[Cl:14][C:5]1[N:6]=[N:7][CH:8]=[C:3]([C:2]([F:11])([F:10])[F:1])[CH:4]=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

4

反応物 2

HCID 24813Phosphorus oxychlorideHCID 155100275-(Trifluoromethyl)-2,3-dihydropyridazin-3-one

生成物 1

HCID 592772973-Chloro-5-(trifluoromethyl)pyridazine

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

反応条件

温度
80 °C

実験手順

5-(Trifluoromethyl)pyridazin-3(2H)-one (20.0 g, 111 mmol) was dissolved in 1,4-dioxane (222 mL) and POCl3 (31.0 mL, 333 mmol) added. The reaction was left to stir at 80° C. for 3 h. After consumption of the starting material, the reaction was cooled to room temperature. The reaction mixture was added to ice and quenched with ammonium hydroxide. The aqueous layer was extracted with dichloromethane (×3) and the organic layers combined, dried with magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified by flash chromatography to afford the title compound as an orange oil. 1H NMR (500 MHz, CDCl3) δ 9.37 (s, 1H); 7.76 (s, 1H).

後処理

  1. waitThe reaction was left
  2. customAfter consumption of the starting material
  3. temperaturethe reaction was cooled to room temperature
  4. additionThe reaction mixture was added to ice
  5. customquenched with ammonium hydroxide
  6. extractionThe aqueous layer was extracted with dichloromethane (×3)
  7. dry with materialdried with magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe residue was purified by flash chromatography

出典と根拠

ORDレコード
ord-f4ddc911ac3e4a54bad9f664dda0f152
出典データセット
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08592425B2

反応ノート

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