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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1700478생성일: 2026년 10월 27일

Tetrahydrofuran → 4-Methyl-7-(2-methylphenyl)-5,6,7,8-tetrahydroquinolin-5-one

https://huagongshe.com/reaction/1700478

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물But-2-yn-1-amine hydrochlorideHCID 12599999—
반응물5-(2-Methylphenyl)cyclohexane-1,3-dioneHCID 17606575—
용매TriethylamineHCID 8471—
생성물4-Methyl-7-(2-methylphenyl)-5,6,7,8-tetrahydroquinolin-5-oneHCID 1093396227.9%

반응 단계

To a mixture of 5-(2-methylphenyl)cyclohexane-1,3-dione (1.5 g), 1-amino-2-butyne hydrochloride (0.86 g), molecular sieves 4A (2 g) and tetrahydrofuran (20 ml) was added triethylamine (0.74 g), and the mixture was stirred at room temperature for 1 hour and then refluxed for 17 hours and cooled. Insoluble materials were filtered off. Under reduced pressure, the solvent was evaporated, and the residue was stirred at 220° C. for 4 hours, to which were added ethyl acetate and sodium hydrogen carbonate solution. The organic layer was washed with water and saturated brine, dried with magnesium sulfate and concentrated under reduced pressure, and the residue was purified with silica gel column chromatography (EtOAc/hexane). The resulting crystals were recrystallized from ethyl acetate-hexane to give colorless crystals of 4-methyl-7-(2-methylphenyl)-5,6,7,8-tetrahydroquinolin-5-one (0.52 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06350749B1
출처 데이터셋uspto-grants-2002_02
ORD IDord-f83281d605a8455db1e59cf654f4f318
출처 메모uspto-grants-2002_02