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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,4-DioxaneHCID 31275—
EduktMethyl 3-amino-4-bromobenzoateHCID 3928639—
EduktMethyl 2-hydroxy-5,5-dimethylcyclohex-1-enecarboxylateHCID 54676124—
LösungsmittelWaterHCID 962—
ProduktMethyl 4-bromo-7,7-dimethyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylateHCID 8965589127%

Reaktionsbedingungen

Temperatur130 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09328111B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-63c433ca5a9c4c4d9a7a233410442823
Quellennotizuspto-grants-2016_05