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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413307Generated: October 28, 2026

Ethanolamine → 2-[4-(5-Trifluoromethyl-1H-pyrazol-3-yl)-phenoxy]-ethylamine

https://huagongshe.com/reaction/413307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantWaterHCID 962—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 178505510HCID 178505510—
SolventDimethyl SulfoxideHCID 679—
Product2-[4-(5-Trifluoromethyl-1H-pyrazol-3-yl)-phenoxy]-ethylamineHCID 983518034.3%

Reaction Conditions

Temperature65 °C

Reaction Steps

In a flame-dried, round-bottomed flask, ethanolamine (836 mg, 13.7 mmol) was dissolved in dimethylsulfoxide (2.7 ml), and potassium tert-butoxide (95%, 1.54 g, 13.7 mmol) was added to the solution. This mixture was stirred at about 65° C. for about ten minutes, and then 5-(4-fluoro-phenyl)-3-trifluoromethyl-1H-pyrazole (630 mg, 2.74 mmol) was added. The dark-colored solution was heated to about 85° C. for about eighteen hours, and was then allowed to cool to room temperature. Water was added, and the resulting tan-colored solid was collected by filtration. This crude product was purified by column chromatography (5% methanol/dichloromethane to 20% methanol/dichloromethane) to afford the product as a white solid (255 mg, 25% yield). LRMS ([M+H]+)=272.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566377B2
Source datasetuspto-grants-2003_05
ORD IDord-44a52068054f4ffebf2b622f6635d783
Source noteuspto-grants-2003_05