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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 29654생성일: 2026년 10월 24일

1-(Bromomethyl)-4-(trifluoromethyl)benzene → 4-{2-[({[4-(tert-Butyl)phenyl]methylidene}amino)oxy]ethoxy}-2-{[4-(trifluoromethyl)benzyl]oxy}benzoic acid

https://huagongshe.com/ko/reaction/29654

반응식

참여 물질

역할이름HCID투입량
반응물1-(Bromomethyl)-4-(trifluoromethyl)benzeneHCID 123062—
반응물4-[2-(4-Tert-butyl-benzylideneaminooxy)-ethoxy]-2-hydroxy-benzoic acidHCID 72970989—
생성물4-{2-[({[4-(tert-Butyl)phenyl]methylidene}amino)oxy]ethoxy}-2-{[4-(trifluoromethyl)benzyl]oxy}benzoic acidHCID 72968076—

반응 단계

The title compound was prepared as a white solid from 4-{2-[({[4-(tert-butyl)phenyl]methylidene}amino)oxy]-ethoxy}-2-hydroxybenzoic acid and 4-trifluromethyl benzyl bromide using a procedure similar to that of step 1 of example 6 followed by a procedure similar to that of step 3 of example 1. mp=164.1-164.8° C.; mass spectrum (+APCI, M+H) m/z 516. 1H NMR (400 MHz, DMSO-d6); δ 12.30 (s, 1H), 8.24 (s, 1H), 7.72 (m, 5H), 7.53 (d, 2H), 7.42 (d, 2H), 6.75 (d, 1H), 6.63 (dd, 1H), 5.29 (s, 2H), 4.41 (t, 2H), 4.3 (t, 2H), 1.25 (s, 9H). Elemental analysis: Calcd. for C28H28F3NO5: C, 65.24; H, 5.47; N, 2.72, Found: C, 63.30; H, 5.21; N, 2.68.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07420083B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-ece64afed3624682bd1e2fcf118a7e54
출처 메모uspto-grants-2008_09