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HRID 1687생성일: 2026년 10월 23일

m-Chloroperbenzoic acid → 2-ethyl-3-chloromethylpyridine-N-oxide

https://huagongshe.com/ko/reaction/1687

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물3-(chloromethyl)-2-ethylPyridineHCID 19690958—
용매ChloroformHCID 6212—
생성물2-ethyl-3-chloromethylpyridine-N-oxideHCID 19690998—

반응 조건

온도0 °C

반응 단계

The 2-ethyl-3-chloromethylpyridine (2.4 g, 15.4 mmol) was dissolved in CHCl3 (100 mL) and cooled under nitrogen to 0° C. and m-chloroperbenzoic acid (55%, 4.2 g) was added in small portions. The reaction was stirred for 2 hours. The reaction was extracted twice with saturated aqueous sodium bicarbonate (100 mL). The organic phase was dried with MgSO4, filtered and the solvent was removed under reduced pressure. The residue was chromatographed on silica gel packed in 98:2 CH2Cl2 :MeOH and eluted with the same. The appropriate fractions were combined and the solvent removed under reduced pressure the give the desired 2-ethyl-3-chloromethylpyridine-N-oxide.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726172
출처 데이터셋uspto-grants-1998_03
ORD IDord-50b5f885709f4236b5aee536d764bea9
출처 메모uspto-grants-1998_03