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HRID 237479作成日:2026年10月25日

Pyridine → 2-(2-Oxopyrrolidin-1-yl)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/237479

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物1-(2-Hydroxyethyl)-2-pyrrolidinoneHCID 76980—
溶媒DichloromethaneHCID 6344—
生成物2-(2-Oxopyrrolidin-1-yl)ethyl 4-methylbenzenesulfonateHCID 44791207—

反応手順

p-Toluenesulfonylchloride (1 g) is added portionwise to a solution of 1-(2-hydroxyethyl)pyrrolidin-2-one (500 μL) and pyridine (1.5 mL) in dichloromethane (8 mL) chilled in an ice bath. The mixture is stirred at room temperature for 12 hours and partitioned between 1 M hydrochloric acid and diethylether. The organic phase is dried (MgSO4) and concentrated. The residue is chromatographed on silica gel (ethyl acetate) to give the title compound. Yield: 390 mg; Mass spectrum (ESI+): m/z=284 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08642585B2
出典データセットuspto-grants-2014_02
ORD IDord-4062c828a452496db321125cd9fbf4e9
出典メモuspto-grants-2014_02