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HRID 54731作成日:2026年10月26日

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

https://huagongshe.com/reaction/54731

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物4-Bromo-1,1,2-trifluorobut-1-eneHCID 66333—
反応物Phthalimide potassium saltHCID 24194345—
反応物3,4,4-Trifluoro-3-butene tosylateHCID 86748462—
触媒Benzenesulfonic acid, 4-methyl-, silver(1+) salt (1:1)HCID 85606—
溶媒DimethylformamideHCID 6228—
溶媒AcetonitrileHCID 6342—
生成物N-(3,4,4-trifluoro 3-butenyl)phthalimideHCID 1523914380.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05623084
出典データセットuspto-grants-1997_04
ORD IDord-66387b82f8284715a5725afed114da3f
出典メモuspto-grants-1997_04