反应 #6582

反应方程式

2-(1-adamantyl)ethanol

diisopropylethylamine

1-acetyl-2-n-butyl 5-acetoxymethyl imidazole

triflic anhydride

→

5-acetoxymethyl-1-[2-(1-adamantyl)-ethyl]-2-n-butyl-imidazole

溶剂

methanol chloroform

methylene chloride

methylene chloride

methylene chloride

反应条件

后处理

1. 1
   浓缩concentrated
2. 2
   温度heated on a steam bath with 10% sodium hydroxide (250 ml)
3. 3
   workup.ADDITIONdiluted with 300 ml of water
4. 4
   萃取extracted with methylene chloride
5. 5
   其他dried
6. 6
   过滤filtered
7. 7
   浓缩concentrated
8. 8
   其他to give an oil

实验过程

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.

来源