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Hydrochloric Acid → 4-(Hydroximinomethyl)cinnoline

HRID 255853
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 255853
[CH3:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[N:4][CH:3]=1.Cl.[N:13](OCCCC)=[O:14]>C(O)C>[N:13](=[CH:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[N:5]=[N:4][CH:3]=1)[OH:14]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 313Hydrochloric AcidHCID 10996Butyl nitriteHCID 268434-Methylcinnoline

Produkt 1

HCID 1363937104-(Hydroximinomethyl)cinnoline

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel3×

Versuchsvorschrift

A solution of 1.44 g of 27A in 3 ml of absolute ethanol was added drop-by-drop over 3 minutes to 3.4 ml of stirred absolute ethanol containing 0.9 g of anhydrous hydrogen chloride, at 0° C. The resulting mixture was stirred for 30 minutes, then a solution of 1.03 g of butyl nitrite in 2 ml of absolute ethanol was added drop-by-drop over 3 minutes at 0° C. The mixture was stirred for 30 minutes at 0° C., for 4 hours at room temperature, then stored in a refrigerator overnight. A precipitated solid was collected, washed with a small amount of water, mixed with a saturated potassium bicarbonate solution, and filtered. Recrystallization from water gave 4-(hydroximinomethyl)cinnoline (27B), as a solid, m.p.: 223° C. (with decomposition).

Aufarbeitung

  1. stirringThe mixture was stirred for 30 minutes at 0° C., for 4 hours at room temperature
  2. customstored in a refrigerator overnight
  3. customA precipitated solid was collected
  4. washwashed with a small amount of water
  5. additionmixed with a saturated potassium bicarbonate solution
  6. filtrationfiltered
  7. customRecrystallization from water

Quellen und Nachweise

ORD-Eintrag
ord-ba1e898e4ef54c7482039a0a44f463ab
Quelldatensatz
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04699651

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