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HRID 45241作成日:2026年10月24日

Thiophenol → 2-Chloro-5-(phenylthio)pyridine

https://huagongshe.com/ja/reaction/45241

反応式

関与物質

役割名称HCID仕込み量
反応物ThiophenolHCID 7969—
反応物2-Chloro-5-iodopyridineHCID 4397176—
反応物Sodium MethoxideHCID 10942334—
触媒CopperHCID 23978—
溶媒MethanolHCID 887—
溶媒Sodium HydroxideHCID 14798—
生成物2-Chloro-5-(phenylthio)pyridineHCID 1119539760%

反応条件

温度80 °C

反応手順

A mixture of 3.4 g (14.3 mmol) of 2-chloro-5 iodopyridine, 1.9 g (17.2 mmol) of thiophenol, 0.93 g (17.2 mmol) of sodium methoxide and 0.36 g (5.7 mmol) of copper in 18 mL of MeOH is heated for 12 hours at 80° C. After cooling to room temperature, the medium is taken up in 100 mL of 1N NaOH and the MeOH is evaporated off under reduced pressure. The reaction medium is extracted with EtOAc (2×100 mL), the organic phase is washed with 0.1N NaOH (2×30 mL), and then dried over Na2SO4, concentrated under reduced pressure and purified by chromatography on a column of silica gel, eluting with a cyclohexane/EtOAc mixture (8/2). 1.90 g of 2-chloro-5-(phenylsulfanyl)pyridine are obtained in the form of a white powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08541455B2
出典データセットuspto-grants-2013_09
ORD IDord-54549360e77f43089666cb6f25cc9bf9
出典メモuspto-grants-2013_09