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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1680생성일: 2026년 10월 23일

Thionyl Chloride → 3-(Chloromethyl)-2-methylpyridine

https://huagongshe.com/ko/reaction/1680

반응식

참여 물질

역할이름HCID투입량
반응물Thionyl ChlorideHCID 24386—
반응물(2-Methylpyridin-3-yl)methanolHCID 302564—
용매DichloromethaneHCID 6344—
생성물3-(Chloromethyl)-2-methylpyridineHCID 12243711—

반응 단계

To a stirred solution of 3-hydroxymethyl-2-methylpyridine from Step 1 above (1.00 g, 8.13 mmol) in 40 mL of CH2Cl2 at ambient temperature was added SOCl2 (9.0 mL, 123 mmol). The reaction mixture was stirred for 4 hours, and the solvent and excess SOCl2 were evaporated under reduced pressure. The residue was partitioned between CH2Cl2 and saturated aqueous NaHCO3. The organic layer was separated, and the aqueous layer was washed with additional CH2 Cl2 (2×40 mL). The combined organic layers were evaporated under reduced pressure to give 3-chloromethyl-2-methylpyridine as a pale yellow-brown solid (TLC: Rf =0.85 in 5% MeOH in CH2Cl2 ; FAB MS m/z 142 (M+ +H)).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05726172
출처 데이터셋uspto-grants-1998_03
ORD IDord-b03b7005ae0f4e16a4358a35620a3d77
출처 메모uspto-grants-1998_03