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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6486생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/6486

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoromethanesulfonic anhydrideHCID 67749—
반응물DiisopropylethylamineHCID 81531—
반응물2-(Tricyclo(3.3.1.1'3,7)dec-1-yl)ethanolHCID 110810—
반응물1-Acetyl-2-n-butyl 5-acetoxymethyl imidazoleHCID 19793547—
용매DichloromethaneHCID 6344—
용매Chloroform methanolHCID 21584188—
생성물5-Acetoxymethyl-1-[2-(1-adamantyl)ethyl]2-n-butylimidazoleHCID 19936797—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05248689
출처 데이터셋uspto-grants-1993_09
ORD IDord-4abdcb5f4ce64f6f9dc993a5b72d5eb7
출처 메모uspto-grants-1993_09