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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 641584생성일: 2026년 10월 26일

3-(Trifluoromethyl)aniline → Benzyl 3-oxo-3-{[3-(trifluoromethyl)phenyl]amino}propanoate

https://huagongshe.com/reaction/641584

반응식

참여 물질

역할이름HCID투입량
반응물3-(Trifluoromethyl)anilineHCID 7375—
반응물4-MethylmorpholineHCID 7972—
반응물Diphenyl chlorophosphateHCID 75654—
반응물Benzyl malonateHCID 22247814—
용매TetrahydrofuranHCID 8028—
생성물Benzyl 3-oxo-3-{[3-(trifluoromethyl)phenyl]amino}propanoateHCID 59666221—

반응 단계

mono-Benzyl malonate (10 g) was dissolved in THF (100 ml), 4-methylmorpholine and cooled to −22° C. prior to the slow addition of diphenyl chlorophosphate (14 ml) and 3-trifluoromethyl-phenylamine (19 ml). After the reaction was warmed to rt overnight, it was heated to gently reflux for 0.5 h. After the reaction was cooled to rt, the solid was filtered off. The filtrate was concentrated. EtOAc was added along with 1N HCl solution. The organic layer was washed with NaHCO3 solution (aq) and brine, dried (MgSO4), filtered, and concentrated. Flash chromatography of the resulting residue gave N-(3-trifluoromethyl-phenyl)-malonamic acid benzyl ester (8.0 g): 1H NMR (CDCl3, δppm, 300 mHz) 3.56 (s, 2H), 5.26 (s, 2H), 7.40 (m, 7H), 7.75 (d, 1H), 7.83 (s, 1H), 9.43 (s, br, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696205B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-05e0347d29644926bfb2ad1dffe84085
출처 메모uspto-grants-2010_04