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HRID 1646134作成日:2026年10月27日

Trifluoromethanesulfonic anhydride → 5-Acetoxymethyl-1-[2-(1-adamantyl)ethyl]2-n-butylimidazole

https://huagongshe.com/reaction/1646134

反応式

関与物質

役割名称HCID仕込み量
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物DiisopropylethylamineHCID 81531—
反応物2-(Tricyclo(3.3.1.1'3,7)dec-1-yl)ethanolHCID 110810—
反応物1-Acetyl-2-n-butyl 5-acetoxymethyl imidazoleHCID 19793547—
溶媒DichloromethaneHCID 6344—
溶媒Chloroform methanolHCID 21584188—
生成物5-Acetoxymethyl-1-[2-(1-adamantyl)ethyl]2-n-butylimidazoleHCID 19936797—

反応条件

温度-78 °C

反応手順

A mixture of 2-(1-adamantyl)ethanol (10.7 g and diisopropylethylamine (11 ml) in dichloromethane (70 ml) was added to triflic anhydride (16.75 g) in dichloro methane (70 ml) at -78° C. under argon. After stirring the mixture at -78° C. for 45 minutes, 1-acetyl-2-n-butyl-5-(acetoxymethyl)imidazole in dichloromethane (50 ml) was added and the mixture was allowed to stand at room temperature for 4 days, then concentrated and heated on a steam bath with 10% sodium hydroxide (250 ml), diluted with 300 ml of water, extracted with dichloromethane, dried, filtered and concentrated to give an oil. Chromatography (silica gel) in methanol chloroform gives 5-acetoxymethyl-1-[2-(1-adamantyl)ethyl]-2-n-butylimidazole.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05177096
出典データセットuspto-grants-1993_01
ORD IDord-7f70daf6f9b647a391578ecb610f4f21
出典メモuspto-grants-1993_01