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HRID 340221作成日:2026年10月25日

m-Chloroperbenzoic acid → 3-(benzyloxy)-5-bromopyridine N-oxide

https://huagongshe.com/reaction/340221

反応式

関与物質

役割名称HCID仕込み量
反応物m-Chloroperbenzoic acidHCID 70297—
反応物3-(Benzyloxy)-5-bromopyridineHCID 15389198—
溶媒DichloromethaneHCID 6344—
生成物3-(benzyloxy)-5-bromopyridine N-oxideHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895577B2
出典データセットuspto-grants-2014_11
ORD IDord-de248117621e4c63ae8d5cb3e3b3d08a
出典メモuspto-grants-2014_11