HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 521399Erstellt: 24. Oktober 2026
1,4-Dioxane → Methyl 4-bromo-7,7-dimethyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylate
https://huagongshe.com/de/reaction/521399
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,4-Dioxane | HCID 31275 | — |
| Edukt | Methyl 3-amino-4-bromobenzoate | HCID 3928639 | — |
| Edukt | Methyl 2-hydroxy-5,5-dimethylcyclohex-1-enecarboxylate | HCID 54676124 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | Methyl 4-bromo-7,7-dimethyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylate | HCID 89655891 | 27% |
Reaktionsschritte
A mixture of methyl 2-hydroxy-5,5-dimethylcyclohex-1-enecarboxylate (26 g, 0.141 mol), methyl 3-amino-4-bromobenzoate (25 g, 0.109 mol), polyphosphoric acid (220 g) and dioxane (220 mL) was heated at 130° C. for 5 hours. After cooling, the mixture was diluted with water. The resulting precipitate was collected by filtration and dried. The solid was suspended in methanol (400 mL), and TMSCl (90 mL) was added. The mixture was stirred at reflux for 5 hours, concentrated and treated with water (80 mL), extracted with ethyl acetate (250 mL). The organic layer was separated, concentrated and recrystallized with methanol to afford desired compound (10.6 g, 27%). 1H NMR (DMSO-d6) δ 10.32 (s, 1H), 7.98 (d, 1H, J=7.2 Hz), 7.10 (d, 1H, J=7.2 Hz), 3.80 (s, 3H), 2.90 (t, 2H, J=6.6 Hz), 2.22 (s, 2H), 1.56 (t, 2H, J=6.6 Hz), and 0.97 (s, 6H). MS (ESI) m/e [M+1]+364.
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-63c433ca5a9c4c4d9a7a233410442823 |
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| Quellennotiz | uspto-grants-2016_05 |
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