制备的基于硫酸的离子液,用于催化转化furfuryl酒精到乙烯基levulinate
Aiyun Hu1,2, Shan Li1, Sheng Zhang1
1Shazhou Professional Institute of Technology, Zhangjiagang, Jiangsu 215600, China.
ACS omega
|April 1, 2024
概括
一种新型的甲硫酸离子液体催化剂[PSna][HSO4],可以高效地将醇转化为乙烯氨酸,产量很高. 这种持久的催化剂在五个循环中表现出极好的可重复使用性,展示了其对可持续化学合成的潜力.
科学领域:
- 绿色化学 绿色化学
- 催化剂是一种催化剂.
- 离子液体是一种离子液体.
背景情况:
- 布伦斯特德酸在有机合成中至关重要.
- 开发高效和稳定的酸催化剂对于可持续的化学过程至关重要.
- 离子液体作为催化介质具有独特的特性.
研究的目的:
- 为了合成一种新型的烯基硫酸离子液体催化剂,[PSna][HSO4].
- 为了评估[PSna][HSO4]的催化性能和稳定性,用于醇转化.
- 通过密度函数理论 (DFT) 的计算来研究反应机制.
主要方法:
- 从尼亚和1,3-propanesulfonic乳中合成[PSna][HSO4]. 在这种过程中,
- 催化测试[PSna][HSO4]在110°C进行2小时的furfuryl酒精转化.
- 催化剂的回收实验最多可以进行五个周期.
- 密度函数理论 (DFT) 计算以阐明反应路径和能量障碍.
主要成果:
- 在最佳条件下实现了97.79%的furfuryl酒精转化和96.10%的乙烯基氨酸产量.
- 证明了催化剂的可重复使用性,在五个周期中保持了高产量 (93.74%的转化率,88.17%的产量).
- DFT计算确定了关键的反应路径和过渡状态.
结论:
- 合成的[PSna][HSO4]是一种高效且稳定的布伦斯特酸催化剂.
- 催化剂具有很好的可回收性,支持其在可持续合成中的应用.
- [PSna][HSO4]为传统的酸催化剂提供了一个有希望的替代品.
相关概念视频
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview
18.0K
The Fischer esterification reaction was developed by the German chemist Emil Fischer in 1895. It is a condensation reaction between carboxylic acids and alcohols in an acidic medium to give esters and water.
18.0K
Acid Halides to Esters: Alcoholysis
2.8K
Alcoholysis is a nucleophilic acyl substitution reaction in which an alcohol functions as a nucleophile. Acid halides react with alcohol to produce esters. The mechanism proceeds in three steps:
2.8K
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism
7.8K
Carboxylic acids react with alcohols to yield esters via an acid-catalyzed condensation reaction called Fischer esterification. This is a nucleophilic acyl substitution reaction that proceeds via a tetrahedral intermediate, where a water molecule is eliminated as the leaving group.
7.8K
Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis
2.8K
Hydrolysis of esters under acidic conditions proceeds through a nucleophilic acyl substitution. In the presence of excess water, the reaction proceeds in a reversible manner, forming carboxylic acids and alcohols.
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
2.8K
Conversion of Alcohols to Alkyl Halides
7.2K
This lesson delves into the conversion of alcohols to corresponding alkyl halides and the mechanism of action for different reagents. Typically, the hydroxyl group is first protonated to convert it to a stable leaving group. Consequently, based on the starting alcohol, the mechanism undergoes either of the nucleophilic substitution routes, SN1 or SN2. Tertiary alkyl halides are made using the two-step SN1 mechanism that occurs via a carbocation intermediate, which is stabilized by...
7.2K
Acid Halides to Carboxylic Acids: Hydrolysis
2.6K
Hydrolysis of acid halides is a nucleophilic acyl substitution reaction in which acid halides react with water to give carboxylic acids. The reaction occurs readily and does not require acid or a base catalyst.
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
As shown below, the mechanism involves a nucleophilic attack by water at the carbonyl carbon to form a tetrahedral intermediate. This is followed by the reformation of the carbon–oxygen π bond along with the departure of a halide ion. A final proton transfer step yields carboxylic...
2.6K


