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HRID 263909Erstellt: 26. Oktober 2026

Water → 9-(2-Methoxyethoxy)-9H-indeno[1,2-b]pyrazine-2,3(1H, 4H)-dione

https://huagongshe.com/reaction/263909

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Eduktp-Toluenesulfonic acidHCID 6101—
Edukt2-MethoxyethanolHCID 8019—
Edukt9-Hydroxy-9H-indeno[1,2-b]pyrazine-2,3(1H,4H)-dioneHCID 19035985—
LösungsmittelBenzeneHCID 241—
Produkt9-(2-Methoxyethoxy)-9H-indeno[1,2-b]pyrazine-2,3(1H, 4H)-dioneHCID 2319405760%

Reaktionsschritte

A suspension of 9-hydroxy-9H-indeno[1,2-b]pyrazine-2,3(1H, 4H)-dione. 1H2O (0.50 g, 2.13 mmol) in benzene (20 ml), 2-methoxyethanol (10 ml) and p-toluensulfonic acid (20 mg) was refluxed with water separation for 20 hours. The reaction mixture was evaporated in vacuo to dryness, the residue was suspended in ethanol (10 ml) and the precipitate was filtered off and washed with ethanol and dried to give 0.48 g of the crude product, which was recrystallized from ethanol to yield 0.35 g (60%) of the title compound. M.p.>300° C. 1 -NMR (DMSO-d6, δ): 3.22 (s, 3H), 3.27-3.51 (m, 4H), 5.24 (s, 1H), 7.18 (t, 1H), 7.33 (t, 1H), 7.42 (d, 1H), 7.5 (d, 1H), 12.06 (s, 1H), 12.29 (s, 1H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05646146
Quelldatensatzuspto-grants-1997_07
ORD IDord-2abaa19444a14684b82adc54b5a29b66
Quellennotizuspto-grants-1997_07