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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(2-(Dimethylamino)ethyl)aniline | HCID 81206 | — |
| Reactant | 5-Methyl-3-phenylisoxazole-4-carbonyl chloride | HCID 85624 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-phenyl-N-(2-dimethylaminoethyl)-5-methyl-3-phenyl-4-isoxazole carboxamide | HCID 13982559 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04681898 |
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| Source dataset | uspto-grants-1987_07 |
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| ORD ID | ord-bbbd39e7ea1b46b3b1dbc5fb251f40f1 |
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| Source note | uspto-grants-1987_07 |
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