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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12646Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3-[4-(Trifluoromethyl)phenyl]-1H-pyrrole-2,5-dione

https://huagongshe.com/de/reaction/12646

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-(Trifluoromethyl)anilineHCID 9964—
EduktMaleimideHCID 10935—
EduktSodium AcetateHCID 517045—
EduktSodium NitriteHCID 23668193—
KatalysatorCupric ChlorideHCID 24014—
LösungsmittelAcetoneHCID 180—
LösungsmittelWaterHCID 962—
Produkt3-[4-(Trifluoromethyl)phenyl]-1H-pyrrole-2,5-dioneHCID 2202689369%

Reaktionsschritte

A mixture of hydrochloric acid (37% in water, 285 mL) and water (190 mL) was added to 4-(trifluoromethyl)aniline (150 g, 116 mL) at room temperature with vigorous stirring and the formed precipitate was allowed to stir for further 30 minutes. Temperature was reduced to 0° C. and sodium nitrite (70.6 g) in 180 mL of water was added dropwise to the stirred suspension. At the end of diazotisation, a clear yellow solution was obtained. Maleimide (180 g) in acetone (1.1 L) was added dropwise at 0° C. and then the pH of the solution was adjusted to 3-3.5 by adding sodium acetate. Copper (II) chloride (18.8 g) was added to the vigorously stirred mixture. After a few minutes a gas started to develop (conspicuous foaming). The reaction mixture was allowed to stir at 0° C. for 1 h and overnight at room temperature. Acetone was removed in vacuo, the residue was filtered and dried overnight in vacuo to give the title compound (155 g) as a light brown solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07727988B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-ef3281565b4e4622afcb19c9b901291b
Quellennotizuspto-grants-2010_06