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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 34912생성일: 2026년 10월 26일

3-Pyridinecarboxaldehyde → 2-Methoxy-5-(pyrid-3-ylhydroxymethyl)pyridine

https://huagongshe.com/reaction/34912

반응식

참여 물질

역할이름HCID투입량
반응물3-PyridinecarboxaldehydeHCID 10371—
반응물Ammonium ChlorideHCID 25517—
반응물5-Bromo-2-methoxypyridineHCID 2734895—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
생성물2-Methoxy-5-(pyrid-3-ylhydroxymethyl)pyridineHCID 1985177823.6%

반응 조건

온도-50 °C

반응 단계

5-Bromo-2-methoxypyridine (188 g) was added over 30 minutes to a 1.55 molar solution of n-butyllithium in hexane (770 ml) and ether (1200 ml) stirred at -50° C. The suspension was stirred for 1 hour when pyridine-3-carboxaldehyde (112 g) in ether (200 ml) was added over 30 minutes. The solution was stirred for 3.5 hr and then allowed to warm to ambient temperature. Saturated ammonium chloride solution (100 ml) and water (2 L) was added and the solution was concentrated to ca. 2.5 L in vacuo. Chloroform (3 L) was added and the title compound (41.3 g) was collected by filtration. The chloroform layer was separated, dried over magnesium sulphate and the solvent was removed under reduced pressure. The residue was treated with chloroform (200 ml) and filtered to give a second crop of the product (51.01 g). Recrystallisation from isopropanol/ether gave the title compound, m.p. 129°-130° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04764519
출처 데이터셋uspto-grants-1988_08
ORD IDord-dc204285c2f4451f98963c40642279f0
출처 메모uspto-grants-1988_08