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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 497168생성일: 2026년 10월 27일

Ethyl trifluoroacetate → Butane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)-

https://huagongshe.com/reaction/497168

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl trifluoroacetateHCID 9794—
반응물HexamethyldisilazaneHCID 13838—
반응물1-(4-(1H-Imidazol-1-yl)phenyl)ethanoneHCID 82316—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물Butane-1,3-dione, 4,4,4-trifluoro-1-(4-imidazol-1-ylphenyl)-HCID 6426099—

반응 조건

온도-78 °C

반응 단계

To a THF (5 mL) solution of 1,1,1,3,3,3-hexamethyldisilazane (0.178 g, 1.1 mmol) was added n-butyl lithum (1.6 M solution in hexane, 0.72 mL, 1.2 mmol) at 0° C. under nitrogen, and the mixture was stirred for 30 minutes, and cooled to −78° C. 4-(1-Imidazolyl)acetophenone (prepared according the method of M. A. Khan et. al., J. Chem. Soc. C., 1970, 85., 0.186 g, 1.0 mmol) was added to the mixture, and residue was stirred for 1 hour. Ethyl trifluoroacetate (0.17 g, 1.2 mmol) was added to the reaction mixture, the residue was warm to room temperature. The reaction mixture was poured into ice water and the whole was extracted with ethyl acetate (30 mL×2). The organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The resulting solid was washed with small amount of ethyl acetate to give the title compound (0.163 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06949536B2
출처 데이터셋uspto-grants-2005_09
ORD IDord-3abc9b509f164373a025f10a80f8e6ad
출처 메모uspto-grants-2005_09