Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1023416Generated: November 3, 2026

Trifluoroacetic acid → HCID 86673604, compound

https://huagongshe.com/reaction/1023416

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant4-Fluorophenylhydrazine hydrochlorideHCID 69981—
ReactantHCID 86673605HCID 86673605—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 86673604HCID 86673604—

Reaction Conditions

Temperature85 °C

Reaction Steps

(4-Fluoro-phenyl)-hydrazine hydrochloride (95 mg, 0.57 mmol) is dissolved in isopropanol (3.0 mL) and triethylamine (0.08 mL, 0.57 mmol) is added. After the mixture is stirred for 5 min, trifluoroacetic acid (0.09 mL, 1.19 mmol) is added and the mixture is again stirred for 5 min Then 1-(2-Chloro-pyridin-4-yl)-4,4,4-trifluoro-butane-1,3-dione (130 mg, 0.52 mmol) is added and the reaction mixture is heated at 85° C. for 40 hrs and stirred at room temperature for another 48 hrs. Water (20 mL) is added and 1.0 M NaOH solution is used to adjust the pH to about 6. The reaction mixture is then extracted with EtOAc (3×20 ml) and the organic layers are combined and concentrated to give the crude product, which is used without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08722709B2
Source datasetuspto-grants-2014_05
ORD IDord-a858884afd0b44749735fa709bd99a01
Source noteuspto-grants-2014_05