HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 521406Erstellt: 25. Oktober 2026
1,4-Dioxane → Methyl 4-methyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylate
https://huagongshe.com/reaction/521406
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | Cyclohexanecarboxylic acid, 2-oxo-, methyl ester | HCID 170489 | — |
| Edukt | Methyl 3-amino-4-methylbenzoate | HCID 337778 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 4-methyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylate | HCID 89669513 | 31,7% |
Reaktionsschritte
A mixture of methyl 2-oxocyclohexanecarboxylate (1.0 g, 6.4 mmol), methyl 3-amino-4-methylbenzoate (1.06 g, 6.4 mmol), polyphosphoric acid (4 mL) and dioxane (6 mL) was heated at 130° C. for 2 hours. After cooling to room temperature, the mixture was diluted with water (100 mL) and the resulting precipitate was collected by filtration and dried. The solid was suspended in methanol (100 mL) and SOCl2 (10 mL) was added. The mixture was stirred at reflux for 5 hours, concentrated and treated with water (80 mL), extracted with ethyl acetate (3×80 mL). The organic layer was separated, concentrated to give the crude product. Then the mixture was purified by chromatography column on silica gel (eluted with CH2Cl2/MeOH) to afford crude product, and the final product (0.55 g) was obtained from recrystallization using MeOH as solvent. 1H NMR (DMSO-d6) δ 10.3 (s, 1H), 7.41 (d, 1H, J=7.8 Hz), 6.99 (d, 1H, J=7.8 Hz), 3.73 (s, 3H), 2.78-2.81 (m, 2H), 2.50 (s, 3H), 2.35-2.37 (m, 2H), and 1.64-1.73 (m, 4H). MS (ESI) m/e [M+1]+272.0.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09328111B2 |
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| Quelldatensatz | uspto-grants-2016_05 |
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| ORD ID | ord-40aa67c6e29f42c98fda582dab79a74b |
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| Quellennotiz | uspto-grants-2016_05 |
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