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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2039631Generated: October 26, 2026

Trifluoroacetic acid → 5-Oxo-2-trifluoromethyl-5,6,7,8-tetrahydro-quinoline-7-carboxylic acid methyl ester

https://huagongshe.com/reaction/2039631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAmmonium trifluoroacetateHCID 2724268—
ReactantMethyl 3,5-dioxocyclohexane-1-carboxylateHCID 11019285—
Reactant(Z)-4-amino-1,1,1-trifluorobut-3-en-2-oneHCID 11116141—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product5-Oxo-2-trifluoromethyl-5,6,7,8-tetrahydro-quinoline-7-carboxylic acid methyl esterHCID 5785590368%

Reaction Steps

A solution of 3,5-Dioxo-cyclohexanecarboxylic acid methyl ester (3.6 g, 21.16 mmol, preparation as in Journal of the Chemical Society, Perkin Transactions 1 (1976), (13), 1382-4), (Z)-4-Amino-1,1,1-trifluoro-but-3-en-2-one (2.94 g, 21.16 mmol, prepared as in EP 744400 (1996)), trifluoroacetic acid (1.21 g, 10.58 mmol), and ammonium trifluoroacetate (1.39 g, 10.58 mmol) in toluene (50 ml) are heated at reflux temperature in a Dean-Stark apparatus. After reaction completion, the reaction mixture is cooled, diluted with ethyl acetate and then washed successively with saturated aqueous sodium bicarbonate and water. The organic phase is dried over anhydrous sodium sulphate, filtered, and concentrated in vacuo. The residue is purified by flash chromatography, eluting with 4:1 hexane to give the title compound (1.5 g, 68%) as white crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580785B2
Source datasetuspto-grants-2013_11
ORD IDord-f07d11c916464953b4aa28af2c7874f0
Source noteuspto-grants-2013_11