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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350423생성일: 2026년 10월 26일

Trifluoroacetic acid → 4-[N'-(2-chlorophenyl)ureido]-3-methylphenylacetic acid

https://huagongshe.com/reaction/350423

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물tert-butyl 4-[N'-(2-chlorophenyl)ureido]-3-methylphenylacetateHCID 23512001—
용매DichloromethaneHCID 6344—
생성물4-[N'-(2-chlorophenyl)ureido]-3-methylphenylacetic acidHCID 23512049100%

반응 단계

To a stirred solution of tert-butyl 4-[N′-(2-chlorophenyl)ureido]-3-methylphenylacetate (1.57 g, 4.19 mmol) in CH2Cl2 (10 ml) was added TFA (6 ml) at room temperature. After 4 h stirring, the mixture was concentrated in vacuo. The residue was triturated by the addition of water to give 4-[N′-(2-chlorophenyl)ureido]-3-methylphenylacetic acid (1.33 g, 100%) as a yellow powder. mp 243–245° C. (dec.); 1H-NMR (CDCl3) δ 2.24 (s, 3H), 3.47 (s, 2H), 6.99–7.08 (m, 3H), 7.28 (t, J=7.6 Hz, 1H), 7.44 (dt, J=8.0, 2.4 Hz, 1H), 7.66 (dd, J=8.3, 1.9 Hz, 1H), 8.13 (dd, J=6.1, 1.7 Hz, 1H), 8.61 (d, J=6.3 Hz, 2H); MS (ESI), m/z 319 (M++1), 321 (M++3); Anal. Calcd for C16H15ClN2O3.0.7TFA: C, 59.33; H, 4.65; Cl, 10.85; N, 8.57. Found: C, 59.23; H, 4.64; Cl, 10.90; N, 8.40.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179819B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-52ec01c497c44bc1b873e9b0aedd742f
출처 메모uspto-grants-2007_02