Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823998Generated: October 27, 2026

Citric Acid → 3-Bromo-1-(4-fluorophenyl)-1h-1,2,4-triazole

https://huagongshe.com/reaction/1823998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
ReactantAcetic acid;tris(4-fluorophenyl)bismuthaneHCID 11966511—
ReactantHCID 178419478HCID 178419478—
CatalystCupric acetateHCID 8895—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductIsohexane ethyl acetateHCID 2188278140%
Product3-Bromo-1-(4-fluorophenyl)-1h-1,2,4-triazoleHCID 2357113245%

Reaction Conditions

Temperature50 °C

Reaction Steps

A mixture of 3-bromo-1,2,4-1H-triazole (prepared as described in Chemische Berichte 1967, 100, 2250) (1.0 g, 6.76 mmol), tri(4-fluorophenyl)bismuth diacetate (prepared by the method described in Synthetic Communications 1996, 4569) (4.53 g, 7.4 mmol), copper (II) acetate (0.25 g, 20 mol %) and N,N,N′,N′-tetramethylguanidine (1.7 mL, 13.5 mmol) in dry tetrahydrofuran (30 mL) was stirred at 50° C. under a balloon of air for 16 hr. The suspension was poured into water (100 mL) and 1M citric acid (30 mL) to give a suspension of pH 3–4. Ethyl acetate (100 mL) was added and the mixture was filtered through Celite®, washing the filter cake with ethyl acetate (100 mL). The two phases of the filtrate were separated and the organic layer was dried (Na2SO4) and concentrated. Flash column chromatography on silica gel, eluting with 25% then 40% ethyl acetate-isohexane, gave 1-(4-fluorophenyl)-3-bromo-1,2,4-1H-triazole as an off-white solid (0.74 g, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041689B2
Source datasetuspto-grants-2006_05
ORD IDord-62e2e6d0e7264c9690a9bb60752fe81c
Source noteuspto-grants-2006_05