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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 26364Erstellt: 26. Oktober 2026

Phthalic Anhydride → 2-(8-Chloro-2-methylquinolin-5-yl)-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/26364

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhthalic AnhydrideHCID 6811—
Edukt1,2,3-TrichlorobenzeneHCID 6895—
Edukt8-Chloro-2-methylquinolin-5-amineHCID 21322927—
Produkt2-(8-Chloro-2-methylquinolin-5-yl)-1H-isoindole-1,3(2H)-dioneHCID 2132291683,3%

Reaktionsschritte

95 g of trichlorobenzene was added to 23.3 g (0.12 mole) of 8-chloro-5-amino-quinaldine and 18.0 g (0.12 mole) of phthalic anhydride, and the mixture was reacted under reflux for 2 hours at the boiling point. After cooling, the precipitated crystals were separated by filtration, and dried to afford 32 g (0.10 mole) of 8-chloro-5-phthalimidoquinaldine.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04150025
Quelldatensatzuspto-grants-1979_04
ORD IDord-6b48f7d1232f46a9947bdd586f8143d2
Quellennotizuspto-grants-1979_04