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HRID 861551Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/861551

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
Edukt4-Bromo-1,1,2-trifluorobut-1-eneHCID 66333—
EduktPhthalimide potassium saltHCID 24194345—
Edukt3,4,4-Trifluoro-3-butene tosylateHCID 86748462—
KatalysatorBenzenesulfonic acid, 4-methyl-, silver(1+) salt (1:1)HCID 85606—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelAcetonitrileHCID 6342—
ProduktN-(3,4,4-trifluoro 3-butenyl)phthalimideHCID 1523914380,9%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05714517
Quelldatensatzuspto-grants-1998_02
ORD IDord-033b1cc9e61745ef8d8a47b4d68d4bc4
Quellennotizuspto-grants-1998_02