化工社化工社 化学情報印刷レポート · 研究参考用
m-Chloroperbenzoic acid → 3-(benzyloxy)-5-bromopyridine N-oxide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | m-Chloroperbenzoic acid | HCID 70297 | — |
| 反応物 | 3-(Benzyloxy)-5-bromopyridine | HCID 15389198 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 3-(benzyloxy)-5-bromopyridine N-oxide | HCID 58213489 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08895577B2 |
| 出典データセット | uspto-grants-2014_11 |
| ORD ID | ord-de248117621e4c63ae8d5cb3e3b3d08a |
| 出典メモ | uspto-grants-2014_11 |