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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517191Generated: October 30, 2026

3-(Trifluoromethyl)aniline → 5-Oxo-3-(3-(trifluoromethyl)phenylamino)cyclohex-3-enecarboxylic acid

https://huagongshe.com/reaction/517191

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Trifluoromethyl)anilineHCID 7375—
ReactantSodium HydroxideHCID 14798—
ReactantYtterbium triflateHCID 2733225—
Reactant3,5-Dioxocyclohexane-1-carboxylic acidHCID 14371458—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Oxo-3-(3-(trifluoromethyl)phenylamino)cyclohex-3-enecarboxylic acidHCID 86732310—

Reaction Steps

A mixture of 3,5-dioxocyclohexanecarboxylic acid (1.00 g, 6.41 mmol), 3-(trifluoromethyl)aniline (880 μL, 1.14 g, 4.05 mmol), Ytterbium(III) trifluormethanesulfonate (20 mg, 32 μmol, 0.5 mol %) and N,N-dimethylformamide (3 mL) is stirred at room temperature over night. Water and aqueous sodium hydroxide are added and the mixture is washed with diethyl ether. The organic layer is discarded, and the aqueous layer is acidified with aqueous hydrogen chloride and extracted with diethyl ether. The organic layer is dried over Na2SO4 and concentrated under reduced pressure. Yield: 1.30 g; ESI mass spectrum [M+H]+=300, Retention time HPLC: 1.08 min (V001—006).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115093B2
Source datasetuspto-grants-2015_08
ORD IDord-e11995f4bf174f3eb075eea376459803
Source noteuspto-grants-2015_08