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HRID 521399作成日:2026年10月26日

1,4-Dioxane → Methyl 4-bromo-7,7-dimethyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylate

https://huagongshe.com/reaction/521399

反応式

関与物質

役割名称HCID仕込み量
反応物1,4-DioxaneHCID 31275—
反応物Methyl 3-amino-4-bromobenzoateHCID 3928639—
反応物Methyl 2-hydroxy-5,5-dimethylcyclohex-1-enecarboxylateHCID 54676124—
溶媒WaterHCID 962—
生成物Methyl 4-bromo-7,7-dimethyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylateHCID 8965589127%

反応条件

温度130 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09328111B2
出典データセットuspto-grants-2016_05
ORD IDord-63c433ca5a9c4c4d9a7a233410442823
出典メモuspto-grants-2016_05