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HRID 54731생성일: 2026년 10월 25일

Ethyl Acetate → N-(3,4,4-trifluoro 3-butenyl)phthalimide

https://huagongshe.com/reaction/54731

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물4-Bromo-1,1,2-trifluorobut-1-eneHCID 66333—
반응물Phthalimide potassium saltHCID 24194345—
반응물3,4,4-Trifluoro-3-butene tosylateHCID 86748462—
촉매Benzenesulfonic acid, 4-methyl-, silver(1+) salt (1:1)HCID 85606—
용매DimethylformamideHCID 6228—
용매AcetonitrileHCID 6342—
생성물N-(3,4,4-trifluoro 3-butenyl)phthalimideHCID 1523914380.9%

반응 단계

To 25 g (0.0896 mole) silver tosylate in 100 mL acetonitrile is slowly added 13.2 g (0.07 mole) 4-bromo-1,1,2-trifluoro-1-butene with stirring, at room temperature. The reaction mixture, protected from the light, is then heated and stirred overnight at reflux. After cooling, the precipitate is filtered off, and the solvent removed from the filtrate under vacuum. Ethyl acetate, 100 mL, is added to the residue of the filtrate and then washed three times with water and dried over magnesium sulfate. To this ethyl acetate solution of 3,4,4-trifluoro-3-butene tosylate is added 25 mL DMF and 16.7 g (0.09 mole) potassium phthalimide. This reaction mixture is stirred at reflux for 24 hrs. After cooling, the precipitate is filtered off and washed with ethyl acetate, which is combined with the filtrate, washed once with water, once with 5% NaOH solution, and then three times with water, and lastly, dried over magnesium sulfate. The solvent is removed under vacuum to yield 14.45 g N-(3,4,4-trifluoro 3-butenyl)phthalimide as a tan solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05623084
출처 데이터셋uspto-grants-1997_04
ORD IDord-66387b82f8284715a5725afed114da3f
출처 메모uspto-grants-1997_04