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Aluminum(III) Chloride → 4-chloro-5-(4-chlorophenyl)-2H-pyridazin-3-one

HRID 2224268
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HRID 2224268 반응식
C([N:8]1[C:13](=[O:14])[C:12]([Cl:15])=[C:11]([C:16]2[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][CH:17]=2)[CH:10]=[N:9]1)C1C=CC=CC=1.[Cl-].[Al+3].[Cl-].[Cl-]>C1(C)C=CC=CC=1>[Cl:15][C:12]1[C:13](=[O:14])[NH:8][N:9]=[CH:10][C:11]=1[C:16]1[CH:17]=[CH:18][C:19]([Cl:22])=[CH:20][CH:21]=1
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참가 물질

4

반응물 2

HCID 6451240Aluminum(III) ChlorideHCID 597166542-benzyl-4-chloro-5-(4-chlorophenyl)pyridazin-3(2H)-one

생성물 1

HCID 597167804-chloro-5-(4-chlorophenyl)-2H-pyridazin-3-one수율 100.2%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
50 °C

실험 절차

2-Benzyl-4-Chloro-5-(4-chloro-phenyl)-2H-pyridazin-3-one (3.19 g, 9.65 mmol) was dissolved in toluene (50 mL). Aluminum chloride (AlCl3, 3.22 g, 24.1 mmol) was then added and the reaction mixture was heated at 50° C. After 20 min, the reaction mixture was cooled to RT and then poured into ice-water (200 mL). The resultant solution was extracted with EtOAc (3×200 mL). The combined organic layers were washed with water (500 mL). The organic layer was dried (MgSO4), filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using EtOAc to give the title compound, 4-chloro-5-(4-chlorophenyl)-2H-pyridazin-3-one (2.33 g) as a white solid. HPLC: 2.74 min.

후처리

  1. temperaturethe reaction mixture was cooled to RT
  2. extractionThe resultant solution was extracted with EtOAc (3×200 mL)
  3. washThe combined organic layers were washed with water (500 mL)
  4. dry with materialThe organic layer was dried (MgSO4)
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customThe residue was purified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-ff69ac71302b43918854a342e1e2632e
출처 데이터셋
uspto-grants-2008_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07378418B2

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