HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Cyclohexylamine → Ethyl 3-(cyclohexylamino)propanoate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Cyclohexylamine | HCID 7965 | — |
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | Ethyl 3-chloropropionate | HCID 69341 | — |
| Katalysator | Tetrabutylammonium Iodide | HCID 67553 | — |
| Produkt | Ethyl 3-(cyclohexylamino)propanoate | HCID 243063 | 72,3% |
Reaktionsbedingungen
| Temperatur | 80 °C |
|---|
Reaktionsschritte
Cyclohexylamine (0.86 g, 8.7 mmol) and 3-chloro-propionic acid ethyl ester (1.18 g, 8.67 mmol) were combined neat and K2CO3 (1.2 g, 8.7 mmol) and a catalytic amount of tetrabutylammonium iodide (ca. 5 mg) was added. The mixture was heated at 80° C. overnight. The resulting mixture was then partitioned between water and DCM. The organic layer was dried (MgSO4) and concentrated to afford 1.25 g (72%) of the title compound. 1H-NMR (400 MHz, CDCl3) δ ppm 4.14 (q, 2H, J=7.2 Hz), 2.90 (t, 2H, J=6.6 Hz), 2.50 (t, 2H, J=6.6 Hz), 1.86-1.89 (m, 2H), 1.70-1.75 (m, 2H), 1.58-1.62 (m, 2H), 1.25 (t, 1H, J=7.2 Hz).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07642270B2 |
| Quelldatensatz | uspto-grants-2010_01 |
| ORD ID | ord-85b7e830fa8d43cbb0d0101ee71686d1 |
| Quellennotiz | uspto-grants-2010_01 |