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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 617806Erstellt: 25. Oktober 2026

Acetic Acid → 4-Oxo-1,2,3,4-tetrahydro-7H-benzo[c]carbazole-8-carboxylic acid

https://huagongshe.com/reaction/617806

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
EduktBenzoic acid, 2-hydrazinyl-, hydrochloride (1:1)HCID 104169—
KatalysatorZincchlorideHCID 3007855—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-Oxo-1,2,3,4-tetrahydro-7H-benzo[c]carbazole-8-carboxylic acidHCID 21849938—

Reaktionsbedingungen

Temperatur85 °C

Reaktionsschritte

5.4 g (28.6 mmol) of 2-hydrazinobenzoic acid hydrochloride and 4.7 g (34.3 mmol) of zinc chloride were added to 300 ml of glacial acetic acid. Under stirring at about 85° C., 4.7 g (28.6 mmol) of the compound of Production Example 6 was added thereto over about 5 minutes. Then the obtained mixture was stirred at the same temperature for about 2 hours, brought back to room temperature and the precipitate was recovered by filtration. After concentrating the filtrate, water was added thereto and the precipitate thus formed was recovered by filtration. These precipitates were combined, dried and then dissolved in about 500 ml of dimethylformamide. Under stirring at room temperature, a solution of 6.5 g (28.6 mmol) of 2,3-dichloro-5,6-dicyano-1,4-benzoquinone in tetrahydrofuran (20 ml) was added thereto and the obtained mixture was stirred for about 30 minutes. After concentrating, about 50 ml of ethanol was added and the precipitate thus formed was recovered by filtration to thereby give 3.4 g of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05952335
Quelldatensatzuspto-grants-1999_09
ORD IDord-8b4671ea111a4c02b29bb02f96d9af51
Quellennotizuspto-grants-1999_09