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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 133749생성일: 2026년 10월 23일

4-Fluoro-3-(trifluoromethyl)phenol → 3-(4-Fluoro-3-trifluoromethylphenoxy)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide

https://huagongshe.com/ko/reaction/133749

반응식

참여 물질

역할이름HCID투입량
반응물4-Fluoro-3-(trifluoromethyl)phenolHCID 601854—
반응물2-Methyl-N-(3-methyl-4-nitrophenyl)oxirane-2-carboxamideHCID 71420003—
생성물3-(4-Fluoro-3-trifluoromethylphenoxy)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamideHCID 67526670—

반응 단계

3-(4-Fluoro-3-trifluoromethylphenoxy)-2-hydroxy-2-methyl-N-(3-methyl-4-nitrophenyl)propionamide was prepared as described in Example 1 starting from 4-fluoro-3-(trifluoromethyl)phenol and 2-methyloxirane-2-carboxylic acid (3-methyl-4-nitrophenyl)amide. The crude product was purified by flash chromatography (dichloromethane-1% methanol). 1H NMR (400 MHz, DMSO-d6): 1.44 (3H, s), 2.53 (3H, s), 4.06 (1H, d, J=9.9 Hz), 4.32 (1H, d, J=9.9 Hz), 6.23 (1H, s), 7.24-7.31 (2H, m), 7.38-7.43 (1H, m), 7.87 (1H, dd, J=9.0 Hz, J=2.1 Hz), 7.91 (1H, d, J=2.0 Hz), 8.03 (1H, d, J=9.0 Hz), 10.14 (1H, s).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07390923B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-52e64b4066d4464ba03414131d32cf32
출처 메모uspto-grants-2008_06