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HRID 1196864作成日:2026年10月27日

Pyridine → 4-[(Chloromethyl)sulfanyl]pyridine

https://huagongshe.com/reaction/1196864

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物ChlorosuccinimideHCID 31398—
反応物4-(Methylthio)pyridineHCID 140938—
溶媒BenzeneHCID 241—
生成物4-[(Chloromethyl)sulfanyl]pyridineHCID 1370398146.5%

反応手順

A solution of 4-methylthiopyridine (2.28 g, 18.2 mmol), N-chlorosuccinimide (3.0 g, 23 mmol) and pyridine (2.9 mL, 3.0 mmol) in benzene (40 mL) was heated at 50°-60° C. for 3 h. The mixture was allowed to cool to room temperature. The solvent was decanted and the residue was rinsed with benzene (2×10 mL). The organic phases were combined and evaporated. The residue was passed through a pad of silica gel (40 g) to give the title material (1.35 g) contaminated with the starting material. The impure product was repurified on silica gel preparative plates (eluted with CH2Cl2 /CH3CN: 1/1) to give the pure title material (926 mg, 32%) as a yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05116833
出典データセットuspto-grants-1992_05
ORD IDord-abb8f79711af4e5884a112e7965ac866
出典メモuspto-grants-1992_05