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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 324139생성일: 2026년 10월 26일

N-methyl-N-(8-phenyloctyl)amine → N-methyl-N-(8-phenyloctyl)-3,5-bis(m-trifluoromethylphenyl)-4-(2-hydroxyethoxy)-benzamide

https://huagongshe.com/reaction/324139

반응식

참여 물질

역할이름HCID투입량
반응물N-methyl-N-(8-phenyloctyl)amineHCID 22237633—
반응물3,5-Bis(m-trifluoromethylphenyl)-4-(2-hydroxyethoxy)benzoic acid ethyl esterHCID 54098193—
생성물N-methyl-N-(8-phenyloctyl)-3,5-bis(m-trifluoromethylphenyl)-4-(2-hydroxyethoxy)-benzamideHCID 22237537—

반응 단계

N-methyl-N-(8-phenyloctyl)-3,5-bis(m-trifluoromethylphenyl)-4-(2-hydroxyethoxy)-benzamide was prepared as a white solid (0.238 g, 67%) from 3,5-bis-(m-trifluoromethylphenyl)-4-(2-hydroxyethoxy)-benzoic acid ethyl ester and N-methyl-N-(8-phenyloctyl)amine using a procedure similar to step 2 of Example 175. 1H NMR (CDCl3) δ7.94 (s, 2H); 7.84 (d, 2H); 7.68-7.56 (m, 4H); 7.44 (s, 2H); 7.30-7.12 (m, 5H); 3.24 (t, 2H); 3.52 and 3.33 (2bt, 2H); 3.40 (t, 2H); 3.08 (2s, 3H); 2.58 (bt, 2H); 1.60 (m, 4H); 1.42-1.12 (m, 8H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06214877B1
출처 데이터셋uspto-grants-2001_04
ORD IDord-da978f1b67304c5094db2fc879e668df
출처 메모uspto-grants-2001_04