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HRID 21377作成日:2026年10月26日

Furan → 2-(4-Chlorobutyl)furan

https://huagongshe.com/reaction/21377

反応式

関与物質

役割名称HCID仕込み量
反応物FuranHCID 8029—
反応物HexaneHCID 8058—
反応物1-Bromo-4-chlorobutaneHCID 81364—
反応物ButyllithiumHCID 178418339—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物2-(4-Chlorobutyl)furanHCID 1329643791%

反応条件

温度-25 °C

反応手順

Furan (1.36 g) was dissolved in tetrahydrofuran (50 ml) and cooled to -25° C. Hexane solution (12.5 ml) of n-butyllithium of 1.68 mol/l was added to the reaction solution, which was stirred at -15° C. for 4 hours. Subsequently, 1-bromo-4-chlorobutane (3.43 g) was dissolved in tetrahydrofuran (2.5 ml) and added to the reaction solution. This solution was further stirred at -15° C. for 1 hour and stood overnight at room temperature. The reaction solution was poured into icy water and extracted with ether. The extracted solution was successively washed with water, a saturated ammonium chloride solution and a saturated sodium chloride solution. It was then dried over magnesium sulfate and filtered. The filtrate was concentrated and the resultant oil-like product was purified by distillation under reduced pressure (130° C./12 mmHg). The object compound (2.87 g) was obtained in the form of oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05422359
出典データセットuspto-grants-1995_06
ORD IDord-c79690b4fafb4e81ad7c25f47c3730a1
出典メモuspto-grants-1995_06