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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426994Generated: November 2, 2026

Trifluoroacetic acid → 4-(4-Fluorophenyl)-1H-pyrazole

https://huagongshe.com/reaction/2426994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 57364150HCID 57364150—
SolventDichloromethaneHCID 6344—
Product4-(4-Fluorophenyl)-1H-pyrazoleHCID 1537648281%

Reaction Steps

A suspension of 4-(4-fluorophenyl)-1-trityl-1H-pyrazole (0.370 g) was suspended in a mixture solution of trifluoroacetic acid (5 ml)/methylene chloride (10 ml) and stirred for 10 min at room temperature, followed by irradiating microwaves thereto at 70° C. for 20 min to induce a reaction. After the reaction was terminated, the solution was diluted in methylene chloride (20 ml), neutralized with 1N sodium hydroxide (20 ml), and washed with distilled water (30 ml) and then with brine (20 ml). The washed organic layer thus formed was dried over anhydrous magnesium sulfate and concentrated by evaporation in a vacuum. The residue thus obtained was separated using silica gel chromatography to give 4-(4-fluorophenyl)-1H-pyrazole (Yield 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968579B2
Source datasetuspto-grants-2011_06
ORD IDord-ac3b8fb84a6c4b4ebc76cc15ec5143ba
Source noteuspto-grants-2011_06