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HRID 1479508作成日:2026年10月27日

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

https://huagongshe.com/reaction/1479508

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US09408907B2
出典データセットuspto-grants-2016_08
ORD IDord-61589c04e9bc4a52aa1ea0921ecefa4c
出典メモuspto-grants-2016_08