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Hydrogen Bromide → 5,8-Quinoxalinediol

HRID 1153729
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1153729
C[O:2][C:3]1[CH:12]=[CH:11][C:10]([O:13]C)=[C:9]2[C:4]=1[N:5]=[CH:6][CH:7]=[N:8]2.Br>C(O)(=O)C>[OH:13][C:10]1[CH:11]=[CH:12][C:3]([OH:2])=[C:4]2[C:9]=1[N:8]=[CH:7][CH:6]=[N:5]2
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 260Hydrogen BromideHCID 600389HCID 600389, Verbindung

Produkt 1

HCID 1356973965,8-Quinoxalinediol

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

Ten grams of 5,8-dimethoxyquinoxaline were dissolved in 100 ml. of glacial acetic acid. After 60 ml. of 48% hydrobromic acid were added to the solution, the reaction was allowed to reflux overnight. The solution was evaporated to dryness in vacuo and a solution of 5% sodium bicarbonate was added until the reaction was basic. The solution was extracted several times with methylene chloride. The combined methylene chloride extracts were dried with sodium sulfate and evaporated to give an amorphous powder which was used without purification for the subsequent reactions.

Aufarbeitung

  1. temperatureto reflux overnight
  2. customThe solution was evaporated to dryness in vacuo
  3. additiona solution of 5% sodium bicarbonate was added until the reaction
  4. extractionThe solution was extracted several times with methylene chloride
  5. dry with materialThe combined methylene chloride extracts were dried with sodium sulfate
  6. customevaporated
  7. customto give an amorphous powder which
  8. customwas used without purification for the subsequent reactions

Quellen und Nachweise

ORD-Eintrag
ord-c2b4993bd13e46808f7ddc4e35a70d2e
Quelldatensatz
uspto-grants-1984_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04486432

Notizen zur Reaktion

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