Réaction #2358518
ord-a6eca46a5fc24a13aa62bbb04e48c19a
Équation de réaction
2-[3-Fluoro-5-(methylsulfonyl)phenoxy]ethanamine
propyl 4-methylbenzenesulfonate
potassium carbonate
→
title compound
Rendement 44.0%
N-{2-[3-fluoro-5-(methylsulfonyl)phenoxy]ethyl}-N-propylamine
Rendement 44.0%
Réactifs
Réactifs
Aucun
Solvants
Conditions de réaction
Température
120°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.
Traitement
- 1AutreThe reaction mixtures
- 2Températurewere cooled to room temperature
- 3Filtrationfiltrated
- 4Autrewere evaporated
- 5AutrePurification by flash column chromatography (ethyl acetate/methanol, 1:0 to 1:1)
Mode opératoire
2-[3-Fluoro-5-(methylsulfonyl)phenoxy]ethanamine (0.3 g, 1.26 mmol), propyl 4-methylbenzenesulfonate D2 (1.04 ml, 12.76 mmol) and potassium carbonate (0.35 g, 2.52 mmol) in acetonitrile (10 ml). The mixture was heated under microwave radiation at 120° C. for 45 min. The reaction mixtures were cooled to room temperature, filtrated and pooled before the volatiles were evaporated. Purification by flash column chromatography (ethyl acetate/methanol, 1:0 to 1:1) gave the title compound (0.15 g, 44%). The amine was converted to the hydrochloric acid salt and re-crystallized from methanol/diethyl ether. MS m/z (relative intensity, 70 eV) 277 (M+, 2), 248 (26), 138 (3), 94 (3), 74 (bp).