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2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → 6-(4-Chloro-1-butenyl)carbostyril

HRID 1285419
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1285419
[Cl:1][CH2:2][CH2:3][CH:4]=[CH:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[NH:12][C:11](=[O:16])[CH2:10][CH2:9]2.ClC1C(=O)C(C#N)=C(C#N)C(=O)C=1Cl>O1CCOCC1.C(Cl)(Cl)Cl.CO>[Cl:1][CH2:2][CH2:3][CH:4]=[CH:5][C:6]1[CH:7]=[C:8]2[C:13](=[CH:14][CH:15]=1)[NH:12][C:11](=[O:16])[CH:10]=[CH:9]2
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Komponenten

6

Edukt 2

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinone2×HCID 544375796-(4-Chloro-1-butenyl)-3,4-dihydrocarbostyril

Produkt 1

HCID 541721066-(4-Chloro-1-butenyl)carbostyril

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 887MethanolLösungsmittelHCID 6212ChloroformLösungsmittel
HCID 31275
1,4-Dioxane
Lösungsmittel

Versuchsvorschrift

2.5 Grams of 6-(4-chloro-1-butenyl)-3,4-dihydrocarbostyril and 2.3 g of DDQ (2,3-dichloro-5,6-dicyanobenzoquinone) were mixed in 160 ml of dioxane and the mixture was refluxed by heating for 6 hours. Further, 1.1 of DDQ was added to the reaction mixture and the mixture was refluxed by heating for 3 hours. The reaction mixture was cooled and the precipitates thus formed were removed by filtration and the mother liquor was concentrated under a reduced pressure to obtain a residue. The residue was dissolved in a mixture of 100 ml of chloroform with 5 ml of methanol and the solution was padded through a silica gel column for removing the unreacted DDQ. The residue was recrystallized from methanol to obtain 1.6 g of 6-(4-chloro-1-butenyl)carbostyril in yellow needle-like crystals. Melting point: 215°-128° C.

Aufarbeitung

  1. temperaturethe mixture was refluxed
  2. temperatureby heating for 6 hours
  3. temperaturethe mixture was refluxed
  4. temperatureby heating for 3 hours
  5. temperatureThe reaction mixture was cooled
  6. customthe precipitates thus
  7. customformed
  8. customwere removed by filtration
  9. concentrationthe mother liquor was concentrated under a reduced pressure
  10. customto obtain a residue
  11. customfor removing the unreacted DDQ
  12. customThe residue was recrystallized from methanol

Quellen und Nachweise

ORD-Eintrag
ord-d17d5a3c470441fe9dff041752d21eaa
Quelldatensatz
uspto-grants-1986_01
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04567187

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