戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 70497作成日:2026年10月27日

Ammonium Chloride → (5-Chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol

https://huagongshe.com/reaction/70497

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium ChlorideHCID 25517—
反応物4-BromothioanisoleHCID 66037—
反応物5-Chloro-6-methoxypicolinaldehydeHCID 58452846—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(5-Chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanolHCID 6739610872.3%

反応手順

n-Butyllithium (2.64 M, 2.9 mL) was added to a solution of 4-bromothioanisole (1.61 g) in tetrahydrofuran (20 mL) at −78° C. in a nitrogen atmosphere, and the mixture was stirred at the same temperature for 30 minutes. A solution of 5-chloro-6-methoxypyridine-2-carbaldehyde (1.14 g) in tetrahydrofuran (10 mL) was added to the reaction solution, followed by stirring for one hour. The reaction solution was poured into a saturated ammonium chloride solution, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered, after which the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=10:1→4:1) to give (5-chloro-6-methoxypyridin-2-yl)[4-(methylsulfanyl)phenyl]methanol as a pale yellow oil (1.42 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822503B2
出典データセットuspto-grants-2014_09
ORD IDord-f806ee9f51c84a7e8397092246675d0c
出典メモuspto-grants-2014_09