HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methyl iodide → tert-butyl N-benzyloxy-N-methylcarbamate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methyl iodide | HCID 6328 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | Tert-butyl N-(benzyloxy)carbamate | HCID 736159 | — |
| Edukt | tert-butyl N-benzyloxy-N-(2-methylpropyl)carbamate | HCID 19967428 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | tert-butyl N-benzyloxy-N-methylcarbamate | HCID 14227181 | — |
Reaktionsschritte
Sodium hydride (0.48 g of 80% in mineral oil, 16 mmol) was added to a solution of tert-butyl N-benzyloxycarbamate (Compound 54 Part A, 3 g, 13 mmol) in N,N-dimethylformamide (25 mL). The reaction mixture was stirred for 20 minutes then iodomethane (1.1 mL, 18 mmol) was added dropwise with cooling in an ice bath. The resulting suspension was stirred at ambient temperature under a nitrogen atmosphere overnight. The reaction mixture was quenched with water (50 mL) then extracted with diethyl ether (150 mL). The organic layer was washed with water (5×50 mL), dried over magnesium sulfate then concentrated to provide 3.1 g of tert-butyl N-benzyloxy-N-methylcarbamate as a yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05612377 |
| Quelldatensatz | uspto-grants-1997_03 |
| ORD ID | ord-3b5ac8a5b1854f79944972dfbdf8fb6b |
| Quellennotiz | uspto-grants-1997_03 |