돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 598959생성일: 2026년 10월 26일

2-Aminothiazole → 5-Fluoro-2-(2-trifluromethylphenoxy)-1-nitrobenzene

https://huagongshe.com/reaction/598959

반응식

참여 물질

역할이름HCID투입량
반응물2-AminothiazoleHCID 2155—
반응물2,5-DifluoronitrobenzeneHCID 67767—
반응물2-TrifluoromethylphenolHCID 67958—
반응물2-(2-Trifluoromethylphenoxy)-5-fluoroanilineHCID 28412097—
생성물n-[5-Fluoro-2-(2-trifluoromethylphenoxy)phenyl]-n'-(thiazol-2-yl)ureaHCID 5973296474%
생성물5-Fluoro-2-(2-trifluromethylphenoxy)-1-nitrobenzeneHCID 6699899278%

반응 단계

5-Fluoro-2-(2-trifluoromethylphenoxy)-1-nitrobenzene (1.17 g, 78%) was prepared from 2-hydroxybenzotrifluoride (0.89 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure A. This compound was reduced to 5-fluoro-2-(2-trifluoromethylphenoxy)-aniline (0.65 g, 62%) following the general procedure B. N-[5-Fluoro-2-(2-trifluoromethylphenoxy)phenyl]-N′-(thiazol-2-yl)urea (146 mg, 74%) was prepared from 2-(2-trifluoromethylphenoxy)-5-fluoroaniline (135 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07897628B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-70714b9f684b4631a985f8ea0bd065ab
출처 메모uspto-grants-2011_03