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

HRID 2046391
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HRID 2046391 반응식
[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
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참가 물질

4

반응물 2

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

생성물 1

HCID 592772973-Chloro-5-(trifluoromethyl)pyridazine

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
80 °C

실험 절차

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).

후처리

  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

출처 및 근거

ORD 기록
ord-f4ddc911ac3e4a54bad9f664dda0f152
출처 데이터셋
uspto-grants-2013_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08592425B2

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