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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912864Generated: October 31, 2026

Potassium Carbonate → 4-(4-methylpiperazin-1-yl)-3-(trifluoromethyl)aniline

https://huagongshe.com/reaction/1912864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-MethylpiperazineHCID 53167—
Reactant2-Fluoro-5-nitrobenzotrifluorideHCID 94954—
ReactantSodium BicarbonateHCID 516892—
SolventDimethylformamideHCID 6228—
Product4-(4-methylpiperazin-1-yl)-3-(trifluoromethyl)anilineHCID 650040094%

Reaction Conditions

Temperature70 °C

Reaction Steps

In 10 mL of dimethylformamide, 300 mg (1.44 mmol) of 2-fluoro-5-nitrobenzotrifluoride was dissolved, and 287 mg (2.88 mmol) of 4-methylpiperazine and 792 mg (5.76 mmol) of potassium carbonate were added thereto and the mixture solution was heated at 70° C. for three hours with vigorous stirring. After cooling, the reaction solution was poured into a saturated sodium bicarbonate solution and extracted with ethyl acetate, and the extract was washed with a saturated sodium chloride solution, and the obtained organic layer as such was used as a substrate in the subsequent catalytic reduction. To the organic layer, 10 mg of 10% palladium carbon was added and the mixture was stirred at room temperature for 16 hours in a hydrogen atmosphere at normal pressures. The catalyst was removed by filtration and the filtrate was concentrated and purified by silica gel column chromatography to obtain 350 mg (94%) of a target product as a brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08609656B2
Source datasetuspto-grants-2013_12
ORD IDord-e26a90c1e3ea42dcad80ad25d4d088cf
Source noteuspto-grants-2013_12