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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| 반응물 | 4-Methylmorpholine | HCID 7972 | — |
| 반응물 | Diphenyl chlorophosphate | HCID 75654 | — |
| 반응물 | Benzyl malonate | HCID 22247814 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | Benzyl 3-oxo-3-{[3-(trifluoromethyl)phenyl]amino}propanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07696205B2 |
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| 출처 데이터셋 | uspto-grants-2010_04 |
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| ORD ID | ord-05e0347d29644926bfb2ad1dffe84085 |
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| 출처 메모 | uspto-grants-2010_04 |
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