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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2118985Generated: October 26, 2026

Triethylamine → N-phenyl-N-(2-dimethylaminoethyl)-5-methyl-3-phenyl-4-isoxazole carboxamide

https://huagongshe.com/reaction/2118985

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantN-(2-(Dimethylamino)ethyl)anilineHCID 81206—
Reactant5-Methyl-3-phenylisoxazole-4-carbonyl chlorideHCID 85624—
SolventTetrahydrofuranHCID 8028—
ProductN-phenyl-N-(2-dimethylaminoethyl)-5-methyl-3-phenyl-4-isoxazole carboxamideHCID 13982559—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 24.6 grams (0.15 mole) of N,N-dimethyl-N'-phenyl-ethylenediamine and 18.2 grams (0.18 mole) of triethylamine in 500 milliliters of tetrahydrofuran (THF) is cooled to 0° C. and 39.8 grams (0.18 mole) of 5-methyl-3-phenyl-4-isoxazole carbonyl chloride in 100 milliliters of tetrahydrofuran is added dropwise. After the addition is complete, the mixture is warmed to room temperature and stirred for 4 hours. The resulting suspension is filtered and the THF removed in vacuo. The residue is dissolved in methylene chloride and washed with 2N sodium hydroxide and water and then dried over magnesium sulfate. The mixture is filtered and the solvent removed by evaporation. The residue is then treated with hexane to yield crystals of N-phenyl-N-(2-dimethylaminoethyl)-5-methyl-3-phenyl-4-isoxazole carboxamide; M.P. 88°-89° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04681898
Source datasetuspto-grants-1987_07
ORD IDord-bbbd39e7ea1b46b3b1dbc5fb251f40f1
Source noteuspto-grants-1987_07