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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1421411Erstellt: 26. Oktober 2026

Diethyl Malonate → Ethyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylate

https://huagongshe.com/reaction/1421411

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl MalonateHCID 7761—
Edukt3-Chloro-2,4-difluorobenzoyl chlorideHCID 2773538—
EduktDiethyl (3-chloro-2,4-difluorobenzoyl)malonateHCID 22077280—
EduktEthyl (3-chloro-2,4-difluoro-benzoyl)-acetateHCID 54232984—
EduktEthyl orthoformate acetic anhydrideHCID 86583744—
ProduktEthyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylateHCID 54286793—

Reaktionsschritte

Reaction of 3-chloro-2,4-difluoro-benzoyl chloride with diethyl malonate gives diethyl (3-chloro-2,4-difluoro-benzoyl)-malonate, and partial hydrolysis and decarboxylation lead to ethyl (3-chloro-2,4-difluoro-benzoyl)-acetate, which is reacted with ethyl orthoformate/acetic anhydride to give ethyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylate; further reaction with cyclopropylamine leads to ethyl 2-(3-chloro-2,4-difluoro-benzoyl)-3-cyclopropylaminoacrylate, which is cyclized with potassium carbonateldimethylformamide to give ethyl 8-chloro-1-cyclopropyl-7-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate; hydrolysis then finally leads to the corresponding carboxylic acid. The reaction sequence described can be represented by the following equation: ##STR4## The quinolonecarboxylic acid obtained in the 6th stage can be converted by reaction with compounds Z--H of the formulae ##STR5## wherein R1 represents hydrogen, straight-chain or branched C1 -C3 -alkyl or cyclopropyl,

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06075165
Quelldatensatzuspto-grants-2000_06
ORD IDord-6b9919477f6547a1aa499d6f7d465975
Quellennotizuspto-grants-2000_06