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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434376Generated: October 25, 2026

Methanol → N-(3-(4-Carbomethoxyphenyl)-1-methylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamine

https://huagongshe.com/reaction/434376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant2-Amino-1-[3-(trifluoromethyl)phenyl]ethan-1-olHCID 30514—
ReactantSodium borohydrideHCID 4311764—
Reactant4-(3-Oxobutyl)benzoic acid methyl esterHCID 10932640—
SolventBenzeneHCID 241—
ProductN-(3-(4-Carbomethoxyphenyl)-1-methylpropyl)-2-hydroxy-2-(3-trifluoromethylphenyl)ethanamineHCID 20493837—

Reaction Steps

A mixture of 4-(4-carbomethoxyphenyl) butan-2-one (3.0 g) and 2-hydroxy-2-(3-trifluoromethylphenyl) ethanamine (3.0 g) in dry benzene (100 ml) was refluxed under Dean and Stark conditions for 2 hours. The solvent was replaced with methanol (100 ml) and sodium borohydride (2.0 g) was added portionwise with ice cooling. The mixture was stirred at ambient temperature for 2 hours, the solvent was evaporated and the residue was partitioned between water (100 ml) and chloroform (100 ml). The organic phase was dried (MgSO4) and evaporated to an oil, which was chromatographed on silica gel 60 in 3% methanol/chloroform. The title compound was obtained as a colourless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04396627
Source datasetuspto-grants-1983_08
ORD IDord-c31c22f76520487db83f593564262688
Source noteuspto-grants-1983_08