HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
m-Chloroperbenzoic acid → 3-(benzyloxy)-5-bromopyridine N-oxide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | m-Chloroperbenzoic acid | HCID 70297 | — |
| Edukt | 3-(Benzyloxy)-5-bromopyridine | HCID 15389198 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-(benzyloxy)-5-bromopyridine N-oxide | HCID 58213489 | — |
Reaktionsschritte
A solution of 3-(benzyloxy)-5-bromopyridine (from step 1) (1.0 eq.) and meta-chloroperbenzoic acid (mCPBA) (4.0 eq.) in dichloromethane (0.1 M) was stirred at room temperature for 18 hours. The reaction was quenched with saturated aqueous NaHCO3 solution and extracted with dichloromethane three times. The combined organic layers were dried over anhydrous MgSO4 and concentrated en vacuo. The crude residue was purified by a COMBIFLASH® system (ISCO) using 0-100% ethyl acetate in hexane to give 3-(benzyloxy)-5-bromopyridine 1-oxide.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08895577B2 |
| Quelldatensatz | uspto-grants-2014_11 |
| ORD ID | ord-de248117621e4c63ae8d5cb3e3b3d08a |
| Quellennotiz | uspto-grants-2014_11 |