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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631844Generated: October 30, 2026

Acetic Acid → HCID 68326436, compound

https://huagongshe.com/reaction/631844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactant3-(Trifluoromethyl)benzaldehydeHCID 67990—
ReactantHCID 68326348HCID 68326348—
CatalystPiperidineHCID 8082—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 68326436HCID 6832643668%

Reaction Steps

3-Oxo-3-(4-phenyl-cyclohexyl)-propionic acid ethyl ester (7) (11.56 g, 42.1 mmol), 3-trifluoromethylbenzaldehyde (11 g, 63.15 mmol), glacial acetic acid (7.16 mmol, 0.41 mL) and piperidine (2.1 mmol, 0.21 mL) were dissolved in toluene (250 mL) and heated under Dean and Stark conditions at reflux for 48 hours. The cooled reaction mixture was diluted with an equal volume of ethyl acetate and washed with 1M aq. HCl and brine. The organics were dried over sodium sulfate, filtered, and evaporated to afford a clear, brown oil. The residue was purified by column chromatography on silica gel (gradient: 0 to 10% tert-butyl methyl ether in cyclohexane) to afford 12.3 g (68%) of (Z)-2-(4-phenylcyclohexanecarbonyl)-3-(3-trifluoromethyl-phenyl)-acrylic acid ethyl ester. 1H NMR (400 MHz, 192191), LCMS (method C), Rt=4.77 min, (M+H)+=431.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321736B2
Source datasetuspto-grants-2016_04
ORD IDord-9d0fac2773d54540a8924a9b7349d92f
Source noteuspto-grants-2016_04