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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Ammonium trifluoroacetate | HCID 2724268 | — |
| Reactant | Methyl 3,5-dioxocyclohexane-1-carboxylate | HCID 11019285 | — |
| Reactant | (Z)-4-amino-1,1,1-trifluorobut-3-en-2-one | HCID 11116141 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Oxo-2-trifluoromethyl-5,6,7,8-tetrahydro-quinoline-7-carboxylic acid methyl ester | HCID 57855903 | 68% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08580785B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-f07d11c916464953b4aa28af2c7874f0 |
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| Source note | uspto-grants-2013_11 |
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