Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234816Erstellt: 25. Oktober 2026

Hydrochloric Acid → 4-(2'-fluoro-5'-chlorophenyl)-4-oxo-2E-butenoic acid

https://huagongshe.com/reaction/234816

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktMaleic AnhydrideHCID 7923—
EduktBenzene, 1-chloro-4-fluoro-HCID 9604—
EduktAluminum(III) ChlorideHCID 6451240—
Produkt4-(2'-fluoro-5'-chlorophenyl)-4-oxo-2E-butenoic acidHCID 10823270—

Reaktionsschritte

Finely pulverized maleic anhydride (3.0 g) is added portionwise to a mixture of 1-chloro-4-fluorobenzene (24.6 g) and anhydrous aluminium chloride (11.56 g). A gas bubbler is attached to the top of the condenser and the mixture is heated in an oil bath at 80°-85° C. for 2 hours at which time little hydrogen chloride gas evolution is evident. The mixture is cooled and the excess 1-chloro-4-fluorobenzene is recovered by distillation at water aspirator pressure. The resultant mixture is quenched with ice and then steam distilled to remove the last traces of the 1-chloro-4-fluorobenzene. Concentrated hydrochloric acid (10 mL) is added to the cooled mixture and the resultant solid collected by filtration (9.2 g). This material is taken up in boiling benzene (50 mL), treated with decolorizing charcoal and filtered through a celite bed. On standing overnight, the yellow solid is collected by filtration (2.45 g). A second recrystallization from benzene (40 mL) leads to 4-(2'-fluoro-5'-chlorophenyl)-4-oxo-2E-butenoic acid (2.1 g) as pure regioisomer.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05596097
Quelldatensatzuspto-grants-1997_01
ORD IDord-ff49ab663d7f4e0ca144a2d5ec31f538
Quellennotizuspto-grants-1997_01