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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350422생성일: 2026년 10월 26일

Chlorophenyl isocyanate → tert-butyl 4-[N'-(2-chlorophenyl)ureido]-3-methylphenylacetate

https://huagongshe.com/reaction/350422

반응식

참여 물질

역할이름HCID투입량
반응물Chlorophenyl isocyanateHCID 76833—
반응물Tert-butyl 4-amino-3-methylphenylacetateHCID 23512173—
용매TetrahydrofuranHCID 8028—
생성물tert-butyl 4-[N'-(2-chlorophenyl)ureido]-3-methylphenylacetateHCID 2351200193%

반응 단계

To a stirred mixture of tert-butyl 4-amino-3-methylphenylacetate (1.00 g, 4.52 mmol), 2-chlorophenyl isocyanate (0.55 ml, 4.52 mmol) in THF (10 ml) was added Et3 N (0.13 ml, 0.90 mmol) at room temperature. After 6 h stirring, the reaction mixture was concentrated in vacuo. The residue was triturated by the addition of n-hexane, to give tert-butyl 4-[N′-(2-chlorophenyl) ureido]-3-methylphenylacetate (1.57 g, 93%) as a pale yellow powder. mp 104–106° C. (dec.); 1H-NMR (CDCl3) δ 1.45 (s, 9H), 2.28 (s, 3H), 3.51 (s, 2H), 6.33 (br, 1H), 6.96 (t, J=7.6 Hz, 1H), 7.08 (br, 1H), 7.16–7.30 (m, 4H), 7.42 (m, 1H), 8.2 (d, J=8.1 Hz, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179819B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-2e2bcdc1888c4ebda7192347bee943c6
출처 메모uspto-grants-2007_02