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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 585363생성일: 2026년 10월 26일

4-Ethoxy-m-anisic acid → 1-(4-Ethoxy-3-methoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinol

https://huagongshe.com/reaction/585363

반응식

참여 물질

역할이름HCID투입량
반응물4-Ethoxy-m-anisic acidHCID 77069—
반응물1,2,3,4-Tetrahydro-2-methyl-4-quinolinolHCID 147634—
반응물4-Ethoxy-3-methoxybenzoyl chlorideHCID 12843153—
용매PyridineHCID 1049—
생성물1-(4-Ethoxy-3-methoxybenzoyl)-2-methyl-1,2,3,4-tetrahydro-4-quinolinolHCID 2233920130%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06930104B2
출처 데이터셋uspto-grants-2005_08
ORD IDord-3cc5cfec28264839b428a7fea88b71be
출처 메모uspto-grants-2005_08