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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1642743Generated: November 3, 2026

Benzoic Acid → 4-[4-(2,4-Dioxo-thiazolidin-5-ylidenemethyl)-2-methoxy-phenoxy]-3-trifluoromethyl-benzonitrile

https://huagongshe.com/reaction/1642743

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
Reactant4-(4-Formyl-2-methoxyphenoxy)-3-(trifluoromethyl)benzonitrileHCID 51051507—
SolventTolueneHCID 1140—
Product4-[4-(2,4-Dioxo-thiazolidin-5-ylidenemethyl)-2-methoxy-phenoxy]-3-trifluoromethyl-benzonitrileHCID 75253234—

Reaction Conditions

Temperature130 °C

Reaction Steps

Thiazolidine-2,4-dione (2.55 g, 21.79 mmol) and 4-(4-Formyl-2-methoxy-phenoxy)-3-trifluoromethyl-benzonitrile (21.79 mmol) were dissolved in toluene (150 mL) and treated with benzoic acid (3.27 mmol) and piperidine (2.83 mmol). The flask was equipped with a Dean-Stark trap, and the reaction was refluxed in a 130° C. oil bath for 12 h. After cooling to RT, the product was collected by filtration and triturated with hexanes to afford the title compound. 1H NMR (400 Hz, DMSO-d6) δ 12.68 (NH), 8.32 (d, 1H), 8.00 (dd, 1H), 7.83 (s, 1H), 7.49 (d, 1H), 7.36 (d, 1H), 7.26 (dd, 1H), 6.90 (d, 1H), 3.77 (s, 3H); LC/MS (m/z) [M+1]+ 421.0 (calculated for C19H12F3N2O4S, 421.04).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08119669B2
Source datasetuspto-grants-2012_02
ORD IDord-33cc1f896f0f47d88e15560b8eae7df3
Source noteuspto-grants-2012_02