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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 350014생성일: 2026년 10월 26일

m-Chloroperbenzoic acid → 5-Phenyl-2-pyridylmethyl acetate

https://huagongshe.com/reaction/350014

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물2-Methyl-5-phenylpyridineHCID 76744—
용매TetrahydrofuranHCID 8028—
생성물5-Phenyl-2-pyridylmethyl acetateHCID 2302506092%

반응 단계

A mixture of 2-methyl-5-phenylpyridine (3.00 g), 3-chloroperbenzoic acid (4.79 g) and tetrahydrofuran (50 ml) was stirred at room temperature overnight, and concentrated. The residue was subjected to silica gel column chromatography to obtain a colorless oily substance from the fraction eluted with tetrahydrofuran. A solution of the resulting colorless oily substance in acetic anhydride (50 ml) was added slowly to acetic anhydride (50 ml) heated at 130° C., which was stirred at 2 hours, and concentrated. The residue was dissolved in ethyl acetate, which was washed with saturated aqueous sodium bicarbonate solution, and with saturated aqueous sodium chloride solution, and then dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography to obtain 5-phenyl-2-pyridylmethyl acetate (3.68 g, yield 92%) as colorless crystals from the fraction eluted with ethyl acetate-hexane (1:2, volume ratio). This was recrystallized from ethyl acetate-hexane. Melting point: 71–72° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179823B1
출처 데이터셋uspto-grants-2007_02
ORD IDord-695e36304ce24f708b060f7f3d7bafad
출처 메모uspto-grants-2007_02