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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 65535생성일: 2026년 10월 23일

3-Methoxybenzaldehyde → 2-Chloro-alpha-(3-methoxyphenyl)-3-pyridinemethanol

https://huagongshe.com/ko/reaction/65535

반응식

참여 물질

역할이름HCID투입량
반응물3-MethoxybenzaldehydeHCID 11569—
반응물3-Bromo-2-chloropyridineHCID 693324—
반응물ButyllithiumHCID 178418339—
반응물HCID 178506730HCID 178506730—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물2-Chloro-alpha-(3-methoxyphenyl)-3-pyridinemethanolHCID 2014573359.8%

반응 단계

71.5 ml of a 2.1N solution of n-butyllithium in hexane are added to 19.2 g 3-bromo-2-chloropyridine (obtained according to J. D. Cook et. al. J. Chem. Soc., Section C, 1969 1973-8) in 300 ml anhydrous ether at -60° C. and under a static nitrogen atmosphere. To this freshly prepared solution of 2-chloro-3-pyridyllithium, a solution of m-anisaldehyde (13.6 g) in 100 ml anhydrous ether is added dropwise. The reaction mixture is stirred for 1 hr. at -60° C. and then is added to ice:water. The organic phase is separated and the aqueous phase is extracted with ether. The combined organic solutions are washed with water, dried (MgSO4) and solvent evaporated. The crude oil is chromatographed over SiO2 and eluted with chloroform, obtaining 14.9 g of title product as an oil which spontaneously crystallises. Recrystallisation from methanol: water affords pure product, m.p. 114°-5° C.; Cl 14.65 (14.20).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04614833
출처 데이터셋uspto-grants-1986_09
ORD IDord-c596dab32d0148ffad05acd071cc1af8
출처 메모uspto-grants-1986_09