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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 521399생성일: 2026년 10월 24일

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

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참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물Methyl 3-amino-4-bromobenzoateHCID 3928639—
반응물Methyl 2-hydroxy-5,5-dimethylcyclohex-1-enecarboxylateHCID 54676124—
용매WaterHCID 962—
생성물Methyl 4-bromo-7,7-dimethyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylateHCID 8965589127%

반응 조건

온도130 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328111B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-63c433ca5a9c4c4d9a7a233410442823
출처 메모uspto-grants-2016_05