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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 519643생성일: 2026년 10월 24일

Trifluoroacetic anhydride → HCID 178438695, 화합물

https://huagongshe.com/ko/reaction/519643

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic anhydrideHCID 9845—
반응물Sodium ThiosulfateHCID 24477—
반응물Hydrogen peroxide waterHCID 449047—
반응물Sodium BicarbonateHCID 516892—
반응물HCID 178438693HCID 178438693—
용매ChloroformHCID 6212—
생성물HCID 178438695HCID 17843869523%

반응 조건

온도60 °C

반응 단계

To a mixture of 4′-{[4-(trans-3-acetylcyclobutyl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile (1.3 g), 30% hydrogen peroxide water (3.5 g) and chloroform (20 mL) was gradually added trifluoroacetic acid anhydride (7.7 mL) at room temperature, and the reaction mixture was warmed to 60° C. and stirred for 24 hr. Saturated aqueous sodium hydrogen carbonate and sodium thiosulfate were added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was dissolved in tetrahydrofuran (10 mL) and methanol (10 mL), 1N aqueous sodium hydroxide solution (5 mL) was added, and the mixture was stirred at room temperature for 30 min. 1N Aqueous hydrochloric acid solution was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to give the title compound as a colorless solid (0.28 g, 23%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09115136B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-e6a2c9044d7d4280a18eea17b3edafd2
출처 메모uspto-grants-2015_08