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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 349977생성일: 2026년 10월 25일

Thionyl Chloride → 5-Chloromethyl-2-(2-phenyl-4-thiazolylmethoxy)pyridine

https://huagongshe.com/reaction/349977

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물2-(2-Phenyl-4-thiazolylmethoxy)-5-pyridylmethanolHCID 22930741—
생성물5-Chloromethyl-2-(2-phenyl-4-thiazolylmethoxy)pyridineHCID 2293078376%

반응 단계

A mixture of 6-(2-phenyl-4-thiazolylmethoxy)-3-pyridylmethanol (2.98 g) and thionyl chloride (15 ml) was stirred at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, and saturated aqueous sodium bicarbonate solution was added to the residue, which was extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4) and concentrated. The residue was subjected to silica gel column chromatography to obtain 5-chloromethyl-2-(2-phenyl-4-thiazolylmethoxy)pyridine (2.40 g, yield 76%) as colorless crystals from the fraction eluted with ethyl acetate. This was recrystallized from tetrahydrofuran-hexane. Melting point: 117–118° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07179823B1
출처 데이터셋uspto-grants-2007_02
ORD IDord-246dea5476394e2fb4a32963b4c8066e
출처 메모uspto-grants-2007_02