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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 865745생성일: 2026년 10월 25일

Carbon Dioxide → N-[4-(Phenylcarbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-trifluoromethyl-propanamide

https://huagongshe.com/reaction/865745

반응식

참여 물질

역할이름HCID투입량
반응물Carbon DioxideHCID 280—
반응물4-AminobenzophenoneHCID 14346—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물3,3,3-Trifluoro-2-hydroxy-2-(trifluoromethyl)propionic AcidHCID 2725043—
용매TetrahydrofuranHCID 8028—
생성물N-[4-(Phenylcarbonyl)phenyl]-3,3,3-trifluoro-2-hydroxy-2-trifluoromethyl-propanamideHCID 21480117—

반응 조건

온도23 °C

반응 단계

Tetrahydrofuran (35 ml,dry) was added to a mixture of 2,2-bis-trifluoromethyl 2-hydroxyacetic acid (1.08 g,5.1 mmol) and 1,1'-carbonyldiimidazole (0.83 g,5.1 mmol), while under a nitrogen atmosphere. There was an immediate evolution of carbon dioxide. The reaction was refluxed for 0.5 hrs and cooled to 23° C. The reaction was treated with 4-aminobenzophenone (1.01 g,5.1 mmol), stirred at 23° C. for 1.5 hrs, and then at reflux 18 hrs. The reaction-was evaporated to a yellow oil-solid mixture. The mixture was dissolved in ethyl ether, treated with hydrogen chloride in ethyl ether, and filtered. The filtrate was evaporated to a yellow oil-solid mixture. Chromatography of this mixture on silica gel, eluting with 5% ethyl ether in methylenechloride provided the title compound as an off-white solid; mp 143°-146° C. 1H-NMR (250 MHz,d6 -DMSO): 7.67(m, 2H, ArH), 7.83(m, 5H, ArH),7.96(d, j=8.8, 2H, ArH), 9.82(s, 1H, OH), 10.82(s, 1H, NH). MS(CI,CH4): 392 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05567735
출처 데이터셋uspto-grants-1996_10
ORD IDord-307ba83f92414e25a0db64e25e75cb95
출처 메모uspto-grants-1996_10