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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 15014생성일: 2026년 10월 24일

p-Toluenesulfonic acid → 2-{6-[2-(2-Chlorophenyl)-5-(4-propoxyphenyl)-pyrrol-1ylmethyl]-2-nitro-pyridin-3-yloxy}-ethanol

https://huagongshe.com/ko/reaction/15014

반응식

참여 물질

역할이름HCID투입량
반응물p-Toluenesulfonic acidHCID 6101—
반응물ChloroformHCID 6212—
반응물1-(2-Chlorophenyl)-4-(4-propoxyphenyl)-butane-1,4-dioneHCID 16090339—
반응물Acetic acid 2-(6-aminomethyl-2-nitropyridin-3-yloxy)-ethyl esterHCID 59341182—
용매2-Methylphenethyl alcoholHCID 88267—
생성물2-{6-[2-(2-Chlorophenyl)-5-(4-propoxyphenyl)-pyrrol-1ylmethyl]-2-nitro-pyridin-3-yloxy}-ethanolHCID 5934120032.6%

반응 조건

온도100 °C

반응 단계

To a solution of 0.2 gm of acetic acid 2-(6-aminomethyl-2-nitropyridin-3-yloxy)-ethyl ester (0.8 mmol) in 3 mL of 5:1 toluene-ethanol was added 0.20 gm of 1-(2-chlorophenyl)-4-(4-propoxyphenyl)-butane-1,4-dione and 10 mg of p-TsOH. The reaction mixture stirred at 100° C. for 72 h. The reaction mixture was poured into 200 mL of CHCl3 and washed twice with water (100 mL), saturated brine, dried (Na2SO4), and the solvents removed under reduced pressure. The residue was purified by column chromatography using 4% methanol-chloroform as an eluent to give 100 mg (25% yield) of an oil. This was used without further purification or characterization.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732457B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-54e07e9af4464f6988cfab1ed5303406
출처 메모uspto-grants-2010_06