Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-Ethoxy-m-anisic acid → 1-(4-Ethoxy-3-methoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-Ethoxy-m-anisic acid | HCID 77069 | — |
| 반응물 | 1,2,3,4-Tetrahydro-2-methyl-4-quinolinol | HCID 147634 | — |
| 반응물 | 4-Ethoxy-3-methoxybenzoyl chloride | HCID 12843153 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | 1-(4-Ethoxy-3-methoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinol | HCID 22339201 | 30% |
반응 단계
2-Methyl-1,2,3,4-tetrahydro-4-quinolinol (7.1 g, 43.5 mmol) synthesized in the published manner was dissolved in pyridine (50 ml), followed by addition of 4-ethoxy-3-methoxybenzoyl chloride prepared from 4-ethoxy-3-methoxybenzoic acid (9.2 g, 46.4 mmol). After stirring at room temperature for 16 hours, the reaction mixture was concentrated and extracted by addition of ethyl acetate and water. After the organic layer was dried and concentrated, the residue was applied to silica gel column chromatography (developing solvent: ethyl acetate/hexane=1/1) and the resulting eluate was recrystallized from ethyl acetate-hexane to give the titled compound (4.4 g, yield: 30%) as a white crystal.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06930104B2 |
| 출처 데이터셋 | uspto-grants-2005_08 |
| ORD ID | ord-3cc5cfec28264839b428a7fea88b71be |
| 출처 메모 | uspto-grants-2005_08 |