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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78368생성일: 2026년 10월 24일

Phenol → 4-(4-(N-methylsulfamoyl)phenoxy)benzene

https://huagongshe.com/ko/reaction/78368

반응식

참여 물질

역할이름HCID투입량
반응물PhenolHCID 996—
반응물4-bromo-N-methylbenzene-1-sulfonamideHCID 101215—
생성물4-(4-(N-methylsulfamoyl)phenoxy)benzeneHCID 23614577—

반응 단계

Entry 54: 4-Bromobenzenesulfonyl chloride was reacted with methylamine according to Method A15, Step 1 to afford N-methyl-4-bromobenzenesulfonamide. N-Methyl-4-bromobenzenesulfonamide was coupled with phenol according to Method A15, Step 2 to afford 4-(4-(N-methylsulfamoyl)phenoxy)benzene. 4-(4-(N-Methylsulfamoyl)phenoxy)benzene was converted into 4-(4-(N-methylsulfamoyl)phenoxy)-1-nitrobenzene according to Method A15, Step 3. 4-(4-(N-Methylsulfamoyl)phenoxy)-1-nitrobenzene was reduced to 4-(4-N-methylsulfamoyl)phenyloxy)aniline according to Method A15, Step 4. According to Method C1a, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-N-methylsulfamoyl)phenyloxy)aniline to afford the urea.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841330B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-54dcfc737e0a4e77bd0ea0e1671e8242
출처 메모uspto-grants-2014_09