HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2118985Erstellt: 23. Oktober 2026
Triethylamine → N-phenyl-N-(2-dimethylaminoethyl)-5-methyl-3-phenyl-4-isoxazole carboxamide
https://huagongshe.com/de/reaction/2118985
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | N-(2-(Dimethylamino)ethyl)aniline | HCID 81206 | — |
| Edukt | 5-Methyl-3-phenylisoxazole-4-carbonyl chloride | HCID 85624 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N-phenyl-N-(2-dimethylaminoethyl)-5-methyl-3-phenyl-4-isoxazole carboxamide | HCID 13982559 | — |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04681898 |
|---|
| Quelldatensatz | uspto-grants-1987_07 |
|---|
| ORD ID | ord-bbbd39e7ea1b46b3b1dbc5fb251f40f1 |
|---|
| Quellennotiz | uspto-grants-1987_07 |
|---|