HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Tert-Butylamine → N-tert-butyl-2-methylpropan-1-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Tert-Butylamine | HCID 6385 | — |
| Edukt | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Edukt | Adiponitrile | HCID 8128 | — |
| Edukt | Potassium Hydroxide | HCID 14797 | — |
| Katalysator | Tetrabutylammonium Iodide | HCID 67553 | — |
| Produkt | N-tert-butyl-2-methylpropan-1-amine | HCID 527145 | — |
Reaktionsschritte
A mixture of tert-butylamine (10.97 g, 0.15 mol), isobutyl bromide (13.70 g, 0.1 mol), adiponitrile (10.81 g, 0.1 mol) and tetrabutylammonium iodide (1.85 g, 5 mmol) was refluxed with stirring for 12 hours. Aqueous 5 M potassium hydroxide (30 ml, 0.15 mmol) was added and the mixture was extracted with n-pentane (2×50 ml). Three layers were formed. Adiponitrile (the middle layer) was recovered. The pentane solution was dried over anhydrous magnesium sulfate and the product was isolated by distillation to yield 9.5 g, (74%), bp 45-47° C./40 mm Hg; 1H NMR (CDCl3) δ0.91 (d, J=6.5 Hz, 6H, CH3), 1.08 (s, 9H, CH3), 1.64 (sep, J=6.5 Hz, 1H, CH), 2.34 (d, J=6.5 Hz, 2H, CH2).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06248885B1 |
| Quelldatensatz | uspto-grants-2001_06 |
| ORD ID | ord-2e6182b2560f49de91847f7ddb264d2c |
| Quellennotiz | uspto-grants-2001_06 |