돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78355생성일: 2026년 10월 24일

2-Methoxy-5-(trifluoromethyl)aniline → 3-(4-Aminophenoxy)benzoic acid

https://huagongshe.com/ko/reaction/78355

반응식

참여 물질

역할이름HCID투입량
반응물2-Methoxy-5-(trifluoromethyl)anilineHCID 600637—
반응물Benzene, 2-isocyanato-1-methoxy-4-(trifluoromethyl)-HCID 11983909—
반응물3-(4-Aminophenoxy)benzoic acidHCID 23009036—
생성물3-(4-Aminophenoxy)benzoic acidHCID 23009036—
생성물N-(5-(trifluoromethyl)-2-methoxyphenyl)-N'-(3-carboxyphenyl)ureaHCID 23614600—

반응 단계

Entry 36: 4-(3-Carboxyphenoxy)aniline was synthesized according to Method A11. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method B1. 4-(3-Carboxyphenoxy)aniline was reacted with 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method C1f to afford N-(5-(trifluoromethyl)-2-methoxyphenyl)-N′-(3-carboxyphenyl)urea, which was coupled with 4-fluoroaniline according to Method D1c.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841330B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-0d6d3c89f2ae44549d4065be26aaac3e
출처 메모uspto-grants-2014_09