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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-(Tricyclo(3.3.1.1'3,7)dec-1-yl)ethanol | HCID 110810 | — |
| 반응물 | 1-Acetyl-2-n-butyl 5-acetoxymethyl imidazole | HCID 19793547 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Chloroform methanol | HCID 21584188 | — |
| 생성물 | 5-Acetoxymethyl-1-[2-(1-adamantyl)ethyl]2-n-butylimidazole | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05248689 |
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| 출처 데이터셋 | uspto-grants-1993_09 |
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| ORD ID | ord-4abdcb5f4ce64f6f9dc993a5b72d5eb7 |
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| 출처 메모 | uspto-grants-1993_09 |
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