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Phosphorus oxychloride → 8-Bromo-4-chloroquinoline

HRID 1403095
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1403095
P(Cl)(Cl)([Cl:3])=O.[Br:6][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:16]=1[NH:15][CH:14]=[CH:13][C:12]2=O>>[Br:6][C:7]1[CH:8]=[CH:9][CH:10]=[C:11]2[C:16]=1[N:15]=[CH:14][CH:13]=[C:12]2[Cl:3]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 24813Phosphorus oxychlorideHCID 124036828-Bromo-1,4-dihydroquinolin-4-one

Produkt 1

HCID 124036918-Bromo-4-chloroquinoline

Versuchsvorschrift

A suspension of 2-bromoaniline (20.9 g) and 5-(methoxymethylene)-2,2-dimethyl-1,3-dioxane-4,6-dione (22.6 g) in 2-propanol (240 ml) was heated to reflux for 1 hour. The reaction solution was cooled to 0° C., and the deposit was then filtrated to obtain a pale yellow solid (35.0 g). A suspension of the obtained pale yellow solid (10.0 g) in Dowtherm (100 ml) was heated at 210° C. for 1 hour. After cooling, hexane (100 ml) was added to the reaction solution, and the deposit was filtrated to obtain 8-bromoquinolin-4(1H)-one (6.3 g). Phosphorus oxychloride (5.9 ml) was added to 8-bromoquinolin-4(1H)-one (9 g), and the mixture was heated to reflux for 2 hours. The solvent was distilled off under reduced pressure, and chloroform was added to the residue. The reaction solution was neutralized with an aqueous sodium hydroxide solution with cooling in an ice bath and partitioned into organic and aqueous layers. The organic layer was washed with brine. The organic layer thus washed was dried over anhydrous sodium sulfate. Then, the solvent was distilled off, and the residue was purified by neutral silica gel column chromatography (chloroform/methanol) to obtain 8-bromo-4-chloroquinoline (8.3 g) as a white solid.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 2 hours
  3. distillationThe solvent was distilled off under reduced pressure, and chloroform
  4. additionwas added to the residue
  5. temperaturewith cooling in an ice bath
  6. custompartitioned into organic and aqueous layers
  7. washThe organic layer was washed with brine
  8. washThe organic layer thus washed
  9. dry with materialwas dried over anhydrous sodium sulfate
  10. distillationThen, the solvent was distilled off
  11. customthe residue was purified by neutral silica gel column chromatography (chloroform/methanol)

Quellen und Nachweise

ORD-Eintrag
ord-f4030206459a410ba87987cf37bb27da
Quelldatensatz
uspto-grants-2014_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08912181B2

Notizen zur Reaktion

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