HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1762806Erstellt: 25. Oktober 2026
Acetic Anhydride → 5,14-Dihydro-2-hydroxy-7-methylbenz[5,6]isoindolo[2,1-b]isoquinoline-8,13-dione
https://huagongshe.com/reaction/1762806
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Acetic Anhydride | HCID 7918 | — |
| Edukt | 1,4-Naphthoquinone | HCID 8530 | — |
| Edukt | 1,2,3,4-Tetrahydro-6-hydroxy-3-isoquinolinecarboxylic acid | HCID 2733174 | — |
| Produkt | 5,14-Dihydro-2-hydroxy-7-methylbenz[5,6]isoindolo[2,1-b]isoquinoline-8,13-dione | HCID 20039736 | — |
Reaktionsschritte
A mixture of 6-hydroxy-1,2,3,4-tetrahydroisoquinoline-3-carboxylic acid (2 g) and 1,4-naphthalenedione (3.4 g) in acetic anhydride (150 ml) was stirred in an oil bath at 100° C. for 15 minutes. It was then allowed to cool to room temperature and the green solid (2.74 g) was collected by filtration, washed with acetic anhydride and ether and dried at 100° C. for 2 h in vacuo, to give the title compound m.p. 275°-320° C. (decomp), λmax (in ethanol) 244.5 nm (ε26,220) 318 nm (ε4,510) and 383 nm (ε6,390).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04835158 |
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| Quelldatensatz | uspto-grants-1989_05 |
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| ORD ID | ord-6198ae7700ac4ce88b270b9d86940696 |
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| Quellennotiz | uspto-grants-1989_05 |
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