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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1099540생성일: 2026년 10월 26일

Trifluoroacetic acid → N-{4-[2-(4-Methoxyphenyl)ethoxy]benzoyl}glycine

https://huagongshe.com/reaction/1099540

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참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물4-Methoxyphenethyl alcoholHCID 69705—
반응물CyanomethylenetributylphosphoraneHCID 4622928—
반응물N-(4-Hydroxybenzoyl)glycine tert-butyl esterHCID 10682169—
용매WaterHCID 962—
용매TolueneHCID 1140—
용매DichloromethaneHCID 6344—
생성물N-{4-[2-(4-Methoxyphenyl)ethoxy]benzoyl}glycineHCID 6681209372%

반응 조건

온도100 °C

반응 단계

(Tributyl phosphoranylidene)acetonitrile (428 μL, 1.50 mmol) was added to a solution of toluene (7 mL) containing N-(4-hydroxybenzoyl)glycine tert-butyl ester (264 mg, 1.05 mmol) prepared in Example 1 (1a) and 2-(4-methoxyphenyl)ethanol (176 mg, 1.16 mmol). The mixture was stirred at 100° C. for 3.5 hours, and then water was added thereto. The mixture was extracted with ethyl acetate. The organic layers were combined, washed with water and saturated brine, and dried over anhydrous magnesium sulfate. Then, the solvent was evaporated. The resulting residue was purified by silica gel column chromatography (hexane to hexane:ethyl acetate, 6:1, 4:1, and 3:1, v/v) to give an oily substance (358 mg). To a solution of dichloromethane (1 mL) containing this oily substance (358 mg, 0.929 mmol), trifluoroacetic acid (0.5 mL) was added. The mixture was stirred at room temperature for 1 hour, and then the solvent was evaporated. Diisopropyl ether was added to the resulting residue to suspend it. The produced precipitate was collected by filtration and was washed with diisopropyl ether to give 248 mg of the title compound (colorless crystalline solid, yield: 72%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08143446B2
출처 데이터셋uspto-grants-2012_03
ORD IDord-c2b5635cc9c646f49e785df05fafb49b
출처 메모uspto-grants-2012_03