Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908217Generated: October 28, 2026

Triethylamine → Ethyl 4-oxo-5-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/1908217

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl 8-chloro-4-oxo-5-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylateHCID 13337379—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl 4-oxo-5-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylateHCID 21829730—

Reaction Conditions

Temperature5 °C

Reaction Steps

A 3-neck, 5-L flask was charged with of ethyl 8-chloro-4-oxo-5-(trifluoromethyl)-1,4-dihydroquinoline-3-carboxylate 15 (100 g, 0.3 mol), ethanol (1250 mL, 12.5 mL/g) and triethylamine (220 mL, 1.6 mol). The vessel was then charged with 10 g of 10% Pd/C (50% wet) at 5° C. The reaction was stirred vigorously under hydrogen atmosphere for 20 h at 5° C., after which time the reaction mixture was concentrated to a volume of approximately 150 mL. The product, ethyl 4-oxo-5-(trifluoromethyl)-1H-quinoline-3-carboxylate 16, as a slurry with Pd/C, was taken directly into the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598205B2
Source datasetuspto-grants-2013_12
ORD IDord-6a77b5e00f4246598a5e268b9324e525
Source noteuspto-grants-2013_12