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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | Methyl 3-amino-4-bromobenzoate | HCID 3928639 | — |
| 반응물 | Methyl 2-hydroxy-5,5-dimethylcyclohex-1-enecarboxylate | HCID 54676124 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | Methyl 4-bromo-7,7-dimethyl-9-oxo-5,6,7,8,9,10-hexahydroacridine-1-carboxylate | HCID 89655891 | 27% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09328111B2 |
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| 출처 데이터셋 | uspto-grants-2016_05 |
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| ORD ID | ord-63c433ca5a9c4c4d9a7a233410442823 |
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| 출처 메모 | uspto-grants-2016_05 |
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