Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzylamine | HCID 7504 | — |
| Edukt | Benzenepropanoic acid, 4-hydroxy-, methyl ester | HCID 79706 | — |
| Lösungsmittel | Hydrochloric Acid | HCID 313 | — |
| Produkt | 3-(4-hydroxyphenyl)-N-benzylpropionamide | HCID 620434 | 98,1% |
Reaktionsschritte
Add benzylamine (32.0 mL, 293 mmol) to methyl 3-(4-hydroxyphenyl)propionate (7.01 g, 38.9 mmol) and heat to 150° C. for 18 h under nitrogen. Cool to room temperature and pour the reaction mixture into 5 N hydrochloric acid (200 mL) and extract with ethyl acetate (3×150 mL). Wash the ethyl acetate extracts with 5 N hydrochloric acid (200 mL), dry the extracts over magnesium sulfate, filter, and concentrate on a rotary evaporator to yield 9.74 g (98%) of N-benzyl-3-(4-hydroxy-phenyl)-propionamide: mass spectrum (ion spray): m/z=256.2 (M+1); 1H NMR (DMSO-d6): 9.15 (s, 1H), 8.28 (t, 1H), 7.39-6.96 (m, 7H), 6.66-6.63 (m, 2H), 4.23 (d, 2H), 2.72 (t, 2H), 2.37 (t, 2H).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07560463B2 |
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| Quelldatensatz | uspto-grants-2009_07 |
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| ORD ID | ord-788b9ffa4e4040d6a4e53ffa0f289b49 |
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| Quellennotiz | uspto-grants-2009_07 |
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