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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2073830Generated: October 31, 2026

Potassium tert-butoxide → Ethyl 1-cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/2073830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178471856HCID 178471856—
Solventtert-ButanolHCID 6386—
ProductEthyl 1-cyclopropyl-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 981754465.1%

Reaction Conditions

Temperature60 °C

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 five 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04920120
Source datasetuspto-grants-1990_04
ORD IDord-cc8b6d01a31e4db38113fca38edac722
Source noteuspto-grants-1990_04