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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212990Generated: October 27, 2026

Formaldehyde → Methyl 2-[3,5-Bis(trifluoromethyl)phenyl]-2-propenoate

https://huagongshe.com/reaction/2212990

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 2-[3,5-bis(trifluoromethyl)phenyl]acetateHCID 10401718—
CatalystTetrabutylammonium IodideHCID 67553—
SolventTolueneHCID 1140—
ProductMethyl 2-[3,5-Bis(trifluoromethyl)phenyl]-2-propenoateHCID 2195518960%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of methyl 3,5-bis(trifluoromethyl)benzeneacetate (Description 1, 10.0 g, 35 mmol), paraformaldehyde (5.2 g, 175 mmol), potassium carbonate (14.5 g, 105 mmol) and tetra-n-butyl ammonium iodide (650 mg, 1.75 mmol) in toluene (200 mL) was heated at 80° C. for 4 hours, cooled and stirred at room temperature for 16 hours. The mixture was filtered through a bed of Celite™, washing with ethyl acetate (2×100 mL). The combined filtrates were washed with water (100 mL) and brine (100 mL), dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with isohexane/EtOAc (100:0 increasing to 90:10) to give the title compound as a clear oil (6.2 g, 60%). 1H NMR (400 MHz, CDCl3) δ 3.86 (3H, s), 6.05 (1H, s), 6.59 (1H, s), 7.86 (1H, s) and 7.88 (2H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07105507B2
Source datasetuspto-grants-2006_09
ORD IDord-eff9bde478cc430097e25718b0c804e4
Source noteuspto-grants-2006_09