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HRID 1259089作成日:2026年10月27日

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

https://huagongshe.com/reaction/1259089

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US08466167B2
出典データセットuspto-grants-2013_06
ORD IDord-ffcc0f99ca19412cb283d8b33d0bbc84
出典メモuspto-grants-2013_06