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Iodine → 6-Iodo-3,4-dihydroquinolin-2(1H)-one

HRID 6812
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 6812
[NH:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH2:4][CH2:3][C:2]1=[O:11].[I:12]I>C(O)C.S([O-])([O-])(=O)=O.[Ag+].[Ag+]>[I:12][C:7]1[CH:6]=[C:5]2[C:10](=[CH:9][CH:8]=1)[NH:1][C:2](=[O:11])[CH2:3][CH2:4]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 2

HCID 807IodineHCID 64796Hydrocarbostyril

Produkt 1

HCID 220189516-Iodo-3,4-dihydroquinolin-2(1H)-one

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 159865Silver sulfateKatalysatorHCID 702EthanolLösungsmittel2×

Versuchsvorschrift

3,4-Dihydroquinolin-2(1H)-one (7.5 g; 51 mmol) and silver (I) sulfate (17.5 g; 56.1 mmol) were suspended in ethanol (250 mL). A solution of iodine in ethanol (250 mL) was added slowly to the reaction over 1 hour. After 6 hours, the reaction was filtered through CELITE diatomaceous earth and washed copiously with methanol. The volatiles were removed under vacuum and the crude residue was triturated with ether. The solids were collected on a fritted funnel and dried under vacuum. This provided the title compound.

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Aufarbeitung

  1. filtrationthe reaction was filtered through CELITE diatomaceous earth
  2. washwashed copiously with methanol
  3. customThe volatiles were removed under vacuum
  4. customthe crude residue was triturated with ether
  5. customThe solids were collected on a fritted funnel
  6. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-d57d16896f9f4187ad5a58a2a543f654
Quelldatensatz
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07084156B2

Notizen zur Reaktion

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