戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 34912作成日:2026年10月26日

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

https://huagongshe.com/reaction/34912

反応式

関与物質

役割名称HCID仕込み量
反応物3-PyridinecarboxaldehydeHCID 10371—
反応物Ammonium ChlorideHCID 25517—
反応物5-Bromo-2-methoxypyridineHCID 2734895—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒Diethyl EtherHCID 3283—
溶媒HexaneHCID 8058—
生成物2-Methoxy-5-(pyrid-3-ylhydroxymethyl)pyridineHCID 1985177823.6%

反応条件

温度-50 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04764519
出典データセットuspto-grants-1988_08
ORD IDord-dc204285c2f4451f98963c40642279f0
出典メモuspto-grants-1988_08