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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856023Generated: October 30, 2026

Water → 2-[N-methyl-(4-trifluoromethoxyphenyl)-amino]ethanol

https://huagongshe.com/reaction/856023

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Bromoethoxy)tetrahydro-2H-pyranHCID 86621—
Reactantn-Methyl-4-(trifluoromethoxy)anilineHCID 737351—
SolventDimethylformamideHCID 6228—
Product2-[N-methyl-(4-trifluoromethoxyphenyl)-amino]ethanolHCID 6947976354.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of N-methyl-(4-trifluoromethoxyphenyl)amine (4.83 g, 24.24 mmol), 2-(2-bromoethoxy)-tetrahydropyran (6.1 g, 29.03 mmol), and potassium carbonate (3.84 g, 27.76 mmol) in DMF (20 ml) was stirred at 100° C. for 5 hours. The reaction mixture was allowed to return to room temperature, poured into water, and extracted with ethyl acetate twice. The extract was washed with water twice and brine, and dried over magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride/ethyl acetate=20/1) to afford 2-[N-methyl-(4-trifluoromethoxyphenyl)-amino]ethanol (3.1 g, yield 53%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-073843149b46452298e48ccbed9587f2
Source noteuspto-grants-2007_08