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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 521406생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/521406

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참여 물질

역할이름HCID투입량
반응물1,4-DioxaneHCID 31275—
반응물Cyclohexanecarboxylic acid, 2-oxo-, methyl esterHCID 170489—
반응물Methyl 3-amino-4-methylbenzoateHCID 337778—
용매WaterHCID 962—
생성물Methyl 4-methyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylateHCID 8966951331.7%

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온도130 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09328111B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-40aa67c6e29f42c98fda582dab79a74b
출처 메모uspto-grants-2016_05