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在无有机溶剂的过程中通过一步添加HO实现α-蒎烯的快速选择性环氧化反应的开发。

Development of rapid and selective epoxidation of α-pinene using single-step addition of HO in an organic solvent-free process.

作者信息

Mukhtar Gunam Resul Mohamad Faiz, Rehman Abdul, López Fernández Ana María, Eze Valentine C, Harvey Adam P

机构信息

School of Engineering, Newcastle University Newcastle upon Tyne NE1 7RU UK.

Department of Chemical and Environmental Engineering, Faculty of Engineering, Universiti Putra Malaysia 43400 UPM Serdang Selangor Malaysia.

出版信息

RSC Adv. 2021 Oct 7;11(52):33027-33035. doi: 10.1039/d1ra05940h. eCollection 2021 Oct 4.

DOI:10.1039/d1ra05940h
PMID:35493558
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9042202/
Abstract

This study reports substantial improvement in the process for oxidising α-pinene, using environmentally friendly HO at high atom economy (∼93%) and selectivity to α-pinene oxide (100%). The epoxidation of α-pinene with HO was catalysed by tungsten-based polyoxometalates without any solvent. The variables in the screening parameters were temperatures (30-70 °C), oxidant amount (100-200 mol%), acid concentrations (0.02-0.09 M) and solvent types (, 1,2-dichloroethane, toluene, -cymene and acetonitrile). Screening the process parameters revealed that almost 100% selective epoxidation of α-pinene to α-pinene oxide was possible with negligible side product formation within a short reaction time (∼20 min), using process conditions of a 50 °C temperature in the absence of solvent and α-pinene/HO/catalyst molar ratio of 5 : 1 : 0.01. A kinetic investigation showed that the reaction was first-order for α-pinene and catalyst concentration, and a fractional order (∼0.5) for HO concentration. The activation energy ( ) for the epoxidation of α-pinene was ∼35 kJ mol. The advantages of the epoxidation reported here are that the reaction could be performed isothermally in an organic solvent-free environment to enhance the reaction rate, achieving nearly 100% selectivity to α-pinene oxide.

摘要

本研究报告了在α-蒎烯氧化过程中取得的显著进展,该过程采用环境友好的HO,具有高原子经济性(约93%)和对α-蒎烯氧化物的选择性(100%)。α-蒎烯与HO的环氧化反应由钨基多金属氧酸盐催化,无需任何溶剂。筛选参数中的变量包括温度(30 - 70°C)、氧化剂用量(100 - 200 mol%)、酸浓度(0.02 - 0.09 M)和溶剂类型(,1,2 - 二氯乙烷、甲苯、对异丙基甲苯和乙腈)。对工艺参数的筛选表明,在50°C的温度、无溶剂以及α-蒎烯/HO/催化剂摩尔比为5∶1∶0.01的工艺条件下,α-蒎烯几乎能100%选择性环氧化生成α-蒎烯氧化物,且在短反应时间(约20分钟)内副产物生成量可忽略不计。动力学研究表明,该反应对α-蒎烯和催化剂浓度为一级反应,对HO浓度为分数级反应(约0.5级)。α-蒎烯环氧化反应的活化能约为35 kJ/mol。此处报道的环氧化反应的优点是,该反应可在无有机溶剂的环境中进行等温反应,以提高反应速率,实现对α-蒎烯氧化物近100%的选择性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/7202af1d176e/d1ra05940h-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/2e96d86a123c/d1ra05940h-f1.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/7cdf293e097a/d1ra05940h-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/1919cf90ace1/d1ra05940h-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/7202af1d176e/d1ra05940h-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/2e96d86a123c/d1ra05940h-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/0eda037a02ac/d1ra05940h-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/a50489c60a42/d1ra05940h-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/11672ba6814e/d1ra05940h-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/7cdf293e097a/d1ra05940h-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/1919cf90ace1/d1ra05940h-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1286/9042202/7202af1d176e/d1ra05940h-f7.jpg

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