돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 27462생성일: 2026년 10월 24일

4-(2-Acetamidoethyl)benzoic acid → 3-Aminobenzoic Acid

https://huagongshe.com/ko/reaction/27462

반응식

참여 물질

역할이름HCID투입량
반응물4-(2-Acetamidoethyl)benzoic acidHCID 343701—
반응물4-(2-Acetaminoethyl)-3-nitro-benzoic acidHCID 23343064—
용매MethanolHCID 887—
생성물3-Aminobenzoic AcidHCID 7419—

반응 단계

4-(2-Acetaminoethyl)-benzoic acid was reacted with nitrating acid to 4-(2-acetaminoethyl)-3-nitro-benzoic acid, M.p. 189° C. (from methanol). The following catalytical hydrogenation yielded the 4-(2-acetaminoethyl)-3-aminoethyl)-3-amino-benzoic acid with a melting point of 143° C. (from ethanol/petroleum ether). From this compound, there was obtained by diazotation and Sandmeyer-reaction the 4-(2-acetamino-ethyl)-3-chloro-benzoic acid having a melting point of 150° C. or by boiling up the diazo solution, the 4-(2-acetaminoethyl)-3-chloro-benzoic acid M.p. 222°-223° C. From 4-(2-acetaminoethyl)-3-hydroxy-benzoic acid, there were obtained with dimethyl sulfate or diethyl sulfate, the corresponding 4-(2-acetaminoethyl)-3-methoxy-benzoic acid methyl ester and the 4-(2-acetaminoethyl)-3-ethoxy-benzoic acid ethyl ester.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04221815
출처 데이터셋uspto-grants-1980_09
ORD IDord-981300d1e03941baa7f21a3dc6806230
출처 메모uspto-grants-1980_09