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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18070생성일: 2026년 10월 25일

6-Chloropyridine-3-carbaldehyde → 2-(Chloropyrid-5-yl)-(4-chlorophenyl)methanol

https://huagongshe.com/reaction/18070

반응식

참여 물질

역할이름HCID투입량
반응물6-Chloropyridine-3-carbaldehydeHCID 2764053—
반응물2-(Chloropyrid-5-yl)-(4-chlorophenyl)bromomethaneHCID 22506785—
반응물HCID 178478191HCID 178478191—
용매TetrahydrofuranHCID 8028—
생성물2-(Chloropyrid-5-yl)-(4-chlorophenyl)methanolHCID 22506792—

반응 단계

2-(Chloropyrid-5-yl)-(4-chlorophenyl)bromo-methane may be prepared by carrying out the procedure in a manner similar to Example 84, starting with 22.5 cm3 of 4-chlorophenylmagnesium bromide (1 M solution in ethyl ether) in 30 cm3 of tetrahydrofuran, under an inert argon atmosphere, and 2.9 g of 2-chloropyridine-5-carboxaldehyde in 30 cm3 of tetrahydrofuran. 3.42 g of 2-(chloropyrid-5-yl)-(4-chlorophenyl)methanol are thus obtained in the form of a pale green powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741316B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ce483d21a0764f32b303eb4437437310
출처 메모uspto-grants-2010_06