HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Butyl iodide → N--t-Butoxycarbonyl-N-butyl-O-benzylhydroxylamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Butyl iodide | HCID 10962 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Tert-butyl N-(benzyloxy)carbamate | HCID 736159 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | N--t-Butoxycarbonyl-N-butyl-O-benzylhydroxylamine | HCID 53942485 | — |
Reaktionsschritte
To a stirred solution at 0° C. of N--t-Butoxycarbonyl-O-benzylhydroxylamine, prepared as in Example 1175A, in anhydrous THF was added portionwise a 60% dispersion of sodium hydride (1.2 equiv.) in mineral oil. Mixture stirred 30 minutes ar 0° C., and then, 1-iodobutane (1.2 equiv.) was added dropwise. Reaction stirred one hour at 0° C., and than, overnight at room temperature. Reaction concentrated in vacuo. Residue taken up in EtOAc and washed with water, 1.0M NaHCO3, 1N H3PO4, and brine. Organic layer dried with Na2SO4, filtered, and evaporated.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06310095B1 |
| Quelldatensatz | uspto-grants-2001_10 |
| ORD ID | ord-7cff57209b0a4774829073d5d421076a |
| Quellennotiz | uspto-grants-2001_10 |