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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36989생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/36989

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 조건

온도-78 °C

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 methylene chloride (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 methylene chloride (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 methylene chloride, 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05418250
출처 데이터셋uspto-grants-1995_05
ORD IDord-8fab5ecdfc72432688ab3105276996ac
출처 메모uspto-grants-1995_05