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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248388Generated: October 25, 2026

Sodium Trifluoroacetate → 1-(4-Methylphenyl)-4-trifluoromethylpyrrole-2-carbonitrile

https://huagongshe.com/reaction/248388

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium TrifluoroacetateHCID 517019—
Reactant1-(4-Methylphenyl)-4-bromo-2-cyanopyrroleHCID 18956250—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(4-Methylphenyl)-4-trifluoromethylpyrrole-2-carbonitrileHCID 1975927027.9%

Reaction Conditions

Temperature200 °C

Reaction Steps

A mixture of 4-bromo-1-(4-methylphenyl)pyrrole-2-carbonitrile (3.66 g), sodium trifluoroacetate (7.62 g), cuprous iodide (5.34 g) and N-methylpyrrolidone (40 ml) was stirred at 200° C. under a nitrogen atmosphere for 11 hours. The mixture was filtered. The filtrate was poured into water and extracted with ethyl acetate twice. The combined organic layer was dried over magnesium sulfate and evaporated in vacuo. The residue was purified by silica gel column chromatography to afford 1-(4-methylphenyl)-4-trifluoromethylpyrrole-2-carbonitrile (0.98 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210092
Source datasetuspto-grants-1993_05
ORD IDord-5d9592eed04d4b8b9906eed4eb778fa5
Source noteuspto-grants-1993_05