HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1081395Generated: November 1, 2026
Potassium tert-butoxide → Ethyl 1-cyclopropyl-6,7,8-trifluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate
https://huagongshe.com/reaction/1081395
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 178471858 | HCID 178471858 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | Ethyl 1-cyclopropyl-6,7,8-trifluoro-5-methyl-1,4-dihydro-4-oxoquinoline-3-carboxylate | HCID 14651259 | 54.9% |
Reaction Steps
To a mixture of 9.05 g (26.3 mmol) of ethyl 2-(2,3,4,5-tetrafluoro-5-methylbenzoyl)-3-cyclopropylaminoacrylate in 100 mL of dry t-butanol was added a slurry of 3.25 g (29.0 mmol) of potassium t-butoxide in 20 mL of dry t-butanol, and the mixture was stirred at 60° C. for 4 hours. The suspension was cooled to room temperature and concentrated to a paste which was partitioned between dichloromethane and 1N hydrochloric acid. The organic layer was separated, dried over magnesium sulfate, and concentrated. Recrystallization from ethyl acetate:hexane gave 4.70 g of the title compound, mp 176°-177° C.
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-cc77184763c0441dba298e0de8b2514c |
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| Source note | uspto-grants-1996_12 |
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