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 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05418250 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-8fab5ecdfc72432688ab3105276996ac |
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| 출처 메모 | uspto-grants-1995_05 |
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