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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953234Generated: October 26, 2026

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

https://huagongshe.com/reaction/1953234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
Reactant3-Chloro-2,4-difluorobenzoyl chlorideHCID 2773538—
ReactantDiethyl (3-chloro-2,4-difluorobenzoyl)malonateHCID 22077280—
ReactantEthyl (3-chloro-2,4-difluoro-benzoyl)-acetateHCID 54232984—
ReactantEthyl orthoformate acetic anhydrideHCID 86583744—
ProductEthyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylateHCID 54286793—

Reaction Steps

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 carbonate/dimethylformamide 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##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114590
Source datasetuspto-grants-2000_09
ORD IDord-82e41766b79e4d9185eb8ecebe068678
Source noteuspto-grants-2000_09