Friedel-Crafts acylation of anisole with octanoic acid over acid modified zeolites

被引:22
|
作者
Bai, Guoyi [1 ]
Han, Jie [1 ]
Zhang, Huanhuan [1 ]
Liu, Chen [1 ]
Lan, Xingwang [1 ]
Tian, Fei [1 ]
Zhao, Zhen [1 ]
Jin, Hui [1 ]
机构
[1] Hebei Univ, Coll Chem & Environm Sci, Key Lab Chem Biol Hebei Prov, Baoding 071002, Peoples R China
来源
RSC ADVANCES | 2014年 / 4卷 / 52期
基金
中国国家自然科学基金;
关键词
CARBOXYLIC-ACIDS; AROMATIC-COMPOUNDS; ALUMINUM DODECATUNGSTOPHOSPHATE; HETEROGENEOUS CATALYSTS; BENZYL ALCOHOL; IONIC LIQUIDS; ALKYLATION; BENZENE; TOLUENE; AGENTS;
D O I
10.1039/c4ra02278e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Friedel-Crafts acylation of anisole using octanoic acid as a green acylating agent was studied over zeolites free of solvent. It was found that a mixed organic acid, composed of tartaric acid and oxalic acid, modified H beta (Mix-H beta) zeolite showed the best catalytic performance among the catalysts studied. The conversion of octanoic acid and the selectivity for p-octanoyl anisole were 72.7% and 82.5%, respectively. Inductively coupled plasma analysis (ICP) and Al-27 MAS NMR indicated dealumination of the parent H beta zeolite due to the treatment of the mixed organic acid, leading to more accessible active sites and accounting for the better catalytic activity of the Mix-H beta zeolite. Furthermore, lower strength of Lewis acid sites and Bronsted acid sites of the Mix-H beta zeolite, as demonstrated by Fourier Transform Infrared Spectrometry after adsorption of pyridine (Py-IR), are advantageous to suppress the demethylation of anisole and the subsequent esterification of thus formed phenol, accounting for its higher selectivity toward p-octanoyl anisole.
引用
收藏
页码:27116 / 27121
页数:6
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