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Water → Ethyl 2,3-dimethylquinoxaline-6-carboxylate

HRID 1498902
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1498902
[NH2:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[NH2:13])[C:5]([O:7][CH2:8][CH3:9])=[O:6].O>C(O)C>[CH3:3][C:2]1[C:12]([CH3:11])=[N:1][C:2]2[C:12](=[CH:11][CH:10]=[C:4]([C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH:3]=2)[N:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 962WaterHCID 458855Ethyl 3,4-Diaminobenzoate

Produkt 1

HCID 2826621Ethyl 2,3-dimethylquinoxaline-6-carboxylateAusbeute 203,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

Ethyl 3,4-diaminobenzoate (500 mg, 2.77 mmol) and diacetyl (238 mg, 2.77 mmol) were dissolved in ethanol (20 ml), and the mixture was heated under reflux. One hour after, diacetyl (30 mg) was added thereto, and the mixture was heated under reflux. After the mixture was heated under reflux for 2.5 hours in total, the reaction solution was poured into water, and the precipitate was separated by filtration and washed with water. By through circulation drying for 15 hours, the title compound (650 mg, quantitative) as a light-brown powder was obtained.

Aufarbeitung

  1. temperaturethe mixture was heated
  2. temperatureunder reflux
  3. additionOne hour after, diacetyl (30 mg) was added
  4. temperaturethe mixture was heated
  5. temperatureunder reflux
  6. temperatureAfter the mixture was heated
  7. temperatureunder reflux for 2.5 hours in total, the reaction solution
  8. customthe precipitate was separated by filtration
  9. washwashed with water
  10. customBy through circulation drying for 15 hours

Quellen und Nachweise

ORD-Eintrag
ord-f07b1b93eab54beaad10684964d97d1c
Quelldatensatz
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09200008B2

Notizen zur Reaktion

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