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Benzene → 4-phenyl-2,5,6,7-tetrahydro-1H-cyclopenta[d]pyridazin-1-one

HRID 469673
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 469673
[C:1]1(=O)[C:5]2[CH2:6][CH2:7][CH2:8][C:4]=2[C:3](=[O:9])O1.[Cl-].[Cl-].[Cl-].[Al+3].O.O.[NH2:17][NH2:18].[CH:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>C(=S)=S.CCO>[C:19]1([C:1]2[C:5]3[CH2:6][CH2:7][CH2:8][C:4]=3[C:3](=[O:9])[NH:17][N:18]=2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 241BenzeneHCID 962WaterHCID 24654Hydrazine hydrate (1:1)HCID 3248541H,3H,4H,5H,6H-cyclopenta(c)furan-1,3-dioneHCID 6451240Aluminum(III) Chloride

Produkt 1

HCID 669665454-phenyl-2,5,6,7-tetrahydro-1H-cyclopenta[d]pyridazin-1-one

Reagenzien, Katalysatoren, Lösungsmittel

2
HCID 702EthanolLösungsmittelHCID 6348Carbon DisulfideLösungsmittel

Versuchsvorschrift

5,6-dihydro-1H-cyclopenta[c]furan-1,3(4H)-dione (1 g, 7 mmol) was added slowly to a well-stirred suspension of aluminum trichloride (1.9 g, 14 mmol) in 15 mL of benzene and 15 mL of CS2. The red reaction mixture was refluxed for 1.5 hours. After cooling, the mixture was poured into water, and extracted with CHCl3. The organic layer was dried (Na2SO4), filtered and concentrated to afford a solid. The solid was dissolved in 20 mL of EtOH, and 5 mL of hydrazine hydrate was added. The mixture was refluxed for 12 hours, allowed to cool, and filtered. The solid collected was washed with water, and dried to afford the title compound. MS (APCI+) M/Z 213 (M+H)+.

Aufarbeitung

  1. customThe red reaction mixture
  2. temperaturewas refluxed for 1.5 hours
  3. temperatureAfter cooling
  4. extractionextracted with CHCl3
  5. dry with materialThe organic layer was dried (Na2SO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto afford a solid
  9. temperatureThe mixture was refluxed for 12 hours
  10. temperatureto cool
  11. filtrationfiltered
  12. customThe solid collected
  13. washwas washed with water
  14. customdried

Quellen und Nachweise

ORD-Eintrag
ord-5dcf3407557344e59c194e575ffd71dd
Quelldatensatz
uspto-grants-2014_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08629143B2

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