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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 338858생성일: 2026년 10월 27일

3-(Trifluoromethyl)aniline → 2-Methyl-7-(trifluoromethyl)quinoline

https://huagongshe.com/reaction/338858

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)anilineHCID 7375—
반응물Ethyl AcetateHCID 8857—
반응물CrotonaldehydeHCID 447466—
용매Hydrochloric AcidHCID 313—
용매WaterHCID 962—
생성물2-Methyl-7-(trifluoromethyl)quinolineHCID 2241690428.9%

반응 단계

To a solution of 3-(trifluoromethyl)aniline (12.43 mL, 99.92 mmol) in 6 N HCl (50 mL) in water was added (E)-but-2-enal (18.77 mL, 229.8 mmol) dropwise at reflux. The reaction was stirred at reflux for 3 hours. After cooling to ambient temperature, ethyl acetate (200 mL) was added. The aqueous layer was separated, basified with ammonium hydroxide to about pH 9, and extracted with DCM (2×200 mL). The combined organic layers were dried (sodium sulfate), filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (5:1 hexane/ethyl acetate) to give 2-methyl-7-(trifluoromethyl)quinoline (6.1 g, 28.9%) as a solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08889704B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-f0ad4393e48c40d8b061304cc8e6b1e3
출처 메모uspto-grants-2014_11