HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2220344Erstellt: 25. Oktober 2026
Phenethylamine → 3-(benzyl-methyl-amino)-N-methoxy-N-methyl-propionamide
https://huagongshe.com/reaction/2220344
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Phenethylamine | HCID 1001 | — |
| Edukt | Acetonitrile | HCID 6342 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 3-bromo-N-methoxy-N-methylpropanamide | HCID 11206373 | — |
| Produkt | 3-(benzyl-methyl-amino)-N-methoxy-N-methyl-propionamide | HCID 59769556 | 82% |
Reaktionsschritte
Add potassium carbonate (63.50 g, 459 mmol) to a stirred solution of N-benzylmethylamine (14.8 mL, 115 mmol), 3-bromo-N-methoxy-N-methyl-propionamide (22.47 g, 115 mmol, prepared according to Jacobi, P. A.; Blum, C. A.; DeSimone, R. W.; Udodong, U. E. S. J. Am. Chem. Soc. 1991, 113, 5384-5392), and anhydrous acetonitrile (460 mL). Heat the reaction to reflux under nitrogen for 3 hours. Cool the reaction to room temperature and filter the reaction through Celite®. Wash the Celite® with ethyl acetate and concentrate on a rotary evaporator to give the crude product. Purify the crude product by flash chromatography on silica gel eluting with 0.5% concentrated ammonium hydroxide/5% ethanol/chloroform to yield 22.31 g (82%) of 3-(benzyl-methyl-amino)-N-methoxy-N-methyl-propionamide: mass spectrum (ion spray) m/z=237.1(M+1); 1H NMR (CDCl3) δ 7.31-7.21 (m, 5H), 3.65 (s, 3H), 3.53 (s, 2H), 3.17 (s, 3H), 2.80-2.76 (m, 2H), 2.67-2.63 (m, 2H), 2.23 (s, 3H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07417064B2 |
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| Quelldatensatz | uspto-grants-2008_08 |
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| ORD ID | ord-48f4ad330ec24a39a8a19fa5e8877132 |
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| Quellennotiz | uspto-grants-2008_08 |
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