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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54432생성일: 2026년 10월 26일

Ethanol → 2-Methyl-4-(4-methylphenyl)-4,6,7,8-tetrahydro-5(1H)-quinolone

https://huagongshe.com/reaction/54432

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물1,3-CyclohexanedioneHCID 10434—
반응물4-(4-Methylphenyl)-3-buten-2-oneHCID 107388—
반응물Ammonium AcetateHCID 517165—
용매Diethyl EtherHCID 3283—
용매Ethyl acetate hexaneHCID 21226206—
생성물2-Methyl-4-(4-methylphenyl)-4,6,7,8-tetrahydro-5(1H)-quinoloneHCID 1995893025.3%

반응 단계

A mixture of 4-(4-methyphenyl)-3-butene-2-one (5.0 g), 1,3-cyclohexanedione (3.66 g), ammonium acetate (3.61 g) and 100 mL of ethanol were heated at reflux overnight and then cooled to room temperature. The solvent was evaporated and the residue was partitioned between water and ethyl acetate. The organic layer was dried, filtered, and evaporated to obtain an amber oil. Chromatography, with hexane:ethyl acetate (1:1) as the eluent, and trituration from ether provided the title compound as an off-white solid (2.0 g); mp 196°-198° C.; NMR: 1.73 (s,3, CH3), 1.87-1.98 (m,2, CH2), 2.14-2.16 (m,2, CH2), 2.22 (s,3, CH3), 2.43-2.49 (m,2, CH2) 4.34 (d,1, CH), 4.57 (d,1, CH), 7.01 (s,4, Ar), 8.40 (s,1, NH); (CI, CH4) MS: m/z=254(M+1). Analysis for C17H19NO: Calculated: C, 80.60; H, 7.56; N, 5.53; Found: C, 80.24; H, 7.68; N, 5.36.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622964
출처 데이터셋uspto-grants-1997_04
ORD IDord-5813a68cf35f46dd87204589308f1001
출처 메모uspto-grants-1997_04