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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 78372생성일: 2026년 10월 24일

Tetrahydrofurfurylamine → 3-(4-Nitrophenoxy)benzoic acid

https://huagongshe.com/ko/reaction/78372

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofurfurylamineHCID 253298—
반응물3-(4-Nitrophenoxy)benzoic acidHCID 767919—
생성물3-(4-Nitrophenoxy)benzoic acidHCID 767919—
생성물3-(4-nitrophenoxy)-N-(tetrahydro-2-furanylmethyl)benzamideHCID 2986507—

반응 단계

Entry 63: 4-(3-Carboxyphenoxy)-1-nitrobenzene was synthesized according to Method A13, Step 2. 4-(3-Carboxyphenoxy)-1-nitrobenzene was coupled with tetrahydrofurfurylamine according to Method A13, Step 3 to give 4-(3-(N-(tetrahydrofurylmethyl)carbamoyl)phenoxy)-1-nitrobenzene. According to Method A13 Step 4, 4-(3-(N-(tetrahydrofurylmethyl)carbamoyl)phenoxy)-1-nitrobenzene was reduced to 4-(3-(N-(tetrahydrofurylmethyl)carbamoyl)phenoxy)aniline. According to Method C1a, 4-chloro-3-(trifluoromethyl)phenyl isocyanate was reacted with 4-(3-(N-(tetrahydrofurylmethyl)carbamoyl)phenoxy)aniline to afford the urea.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08841330B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-960654546b55426a858bdc82374e4060
출처 메모uspto-grants-2014_09