戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 6486作成日:2026年10月25日

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

https://huagongshe.com/reaction/6486

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—

反応手順

A mixture of 2-(1-adamantyl)ethanol (10.7 g) and diisopropylethylamine (11 ml) in methylene chloride (70 ml) was added to triflic anhydride (16.75 g) in 70 ml of methylene chloride at -78° C. for 45 minutes, 1-acetyl-2-n-butyl 5-acetoxymethyl imidazole in 50 ml of methylene chloride 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 methylene chloride, dried, filtered and concentrated to give an oil. Chromatography on silica gel in methanol/chloroform gave 5-acetoxymethyl-1-[2-(1-adamantyl)-ethyl]-2-n-butyl-imidazole. This acetoxy compound (5.4 g) was stirred at room temperature with potassium hydroxide (5.2 g) in ethanol (200 ml) for one hour, the mixture was concentrated, poured into water, stirred, and filtered to give 1-[2-(1-adamantyl)ethyl]-2-n-butyl-5-hydroxymethyl- 1H-imidazole.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248689
出典データセットuspto-grants-1993_09
ORD IDord-4abdcb5f4ce64f6f9dc993a5b72d5eb7
出典メモuspto-grants-1993_09