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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | 3-Chloro-2,4-difluorobenzoyl chloride | HCID 2773538 | — |
| Reactant | Diethyl (3-chloro-2,4-difluorobenzoyl)malonate | HCID 22077280 | — |
| Reactant | Ethyl (3-chloro-2,4-difluoro-benzoyl)-acetate | HCID 54232984 | — |
| Reactant | Ethyl orthoformate acetic anhydride | HCID 86583744 | — |
| Product | Ethyl 2-(3-chloro-2,4-difluorobenzoyl)-3-ethoxy-acrylate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06114590 |
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| Source dataset | uspto-grants-2000_09 |
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| ORD ID | ord-82e41766b79e4d9185eb8ecebe068678 |
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| Source note | uspto-grants-2000_09 |
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