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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266330Generated: October 26, 2026

4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedione → 2-(5-Furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-benzoic acid

https://huagongshe.com/reaction/1266330

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,4,4-Trifluoro-1-(2-furanyl)-1,3-butanedioneHCID 67594—
Reactant2-Hydrazinobenzoic acidHCID 79223—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product2-(5-Furan-2-yl-3-trifluoromethyl-pyrazol-1-yl)-benzoic acidHCID 11415997—

Reaction Steps

4,4,4-Trifluoro-1-(2-furyl)-1,3-butanedione (2.4 mL, 16 mmol) was added to 2-hydrazinobenzoic acid (3.01 g, 16 mmol) in acetic acid (20 mL) and heated at reflux for 25 h. The reaction was cooled, diluted with EtOAc, and extracted twice with water. The organic layer was dried over Na2SO4, filtered, and evaporated to yield a thick red paste (5.71 g, >100%). 1H NMR (CDCl3) δ8.18 (dd, 1H, J=7.7, J′=1.8), 7.74 (td, 1H, J=7.7, J′=1.4), 7.65 (td, 1H, J=7.7, J′=1.5), 7.50 (dd, 1H, J=7.3, J′=1.1), 7.35 (m, 1H), 6.89 (s, 1H), 6.28 (m, 1H), 5.76 (d, 1H, J=3.3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06548525B2
Source datasetuspto-grants-2003_04
ORD IDord-79db81ffe7714050b073a81e99ce3197
Source noteuspto-grants-2003_04