HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081408Generated: November 1, 2026
Potassium tert-butoxide → Ethyl 1-cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate
https://huagongshe.com/reaction/1081408
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178471856 | HCID 178471856 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | Ethyl 1-cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate | HCID 9817544 | 65.1% |
Reaction Steps
A solution of 7.2 g (22 mmol) of ethyl 2-(2,4,5-trifluoro-5-methylbenzoyl)-3-cyclopropylaminoacrylate in 100 mL of dry t-butanol was treated portionwise with 2.8 g (25 mmol) of potassium t-butoxide, and the reaction mixture was stirred at 60° C. for 5 hours. The suspension was cooled to room temperature and concentrated. The residue was partitioned between dichloromethane and 1N hydrochloric acid; the organic phase was washed with water, dried over magnesium sulfate, and concentrated. The crude product was slurried in boiling ethanol, filtered, and air-dried to give 4.2 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05585491 |
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| Source dataset | uspto-grants-1996_12 |
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| ORD ID | ord-0aea4dbcd937491282f71f3c781034b6 |
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| Source note | uspto-grants-1996_12 |
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