Recyclable and reusable Pd(OAc)2/P(1-Nap)3/[bmim][PF6]/H2O system for the addition of arylboronic acids to aldehydes

被引:14
|
作者
Zhao, Hong [1 ,2 ,3 ]
Cheng, Mingzhu [1 ,2 ]
Zhang, Tinli [1 ,2 ]
Cai, Mingzhong [1 ,2 ]
机构
[1] Jiangxi Normal Univ, Minist Educ, Key Lab Funct Small Organ Mol, Nanchang 330022, Peoples R China
[2] Jiangxi Normal Univ, Dept Chem, Nanchang 330022, Peoples R China
[3] Guangdong Pharmaceut Univ, Sch Chem & Chem Engn, Guangzhou 510006, Guangdong, Peoples R China
基金
中国国家自然科学基金;
关键词
Palladium; Ionic liquid; Carbinol; Arylboronic acid; Green chemistry; RHODIUM-CATALYZED ADDITION; TEMPERATURE IONIC LIQUIDS; CROSS-COUPLING REACTIONS; CARBONYL-COMPOUNDS; HIGHLY EFFICIENT; ENANTIOSELECTIVE ADDITION; AROMATIC-ALDEHYDES; ORGANIC-REACTIONS; CARBENE COMPLEX; HECK REACTION;
D O I
10.1016/j.jorganchem.2014.11.020
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
A stable and efficient Pd(OAc)(2)/P(1-Nap)(3)[tri(1-naphthyl)phosphine] catalytic system for the addition of arylboronic acids to aldehydes has been developed. In the presence of Pd(OAc)(2) and P(1-Nap)(3), the addition reaction of arylboronic acids with aldehydes was carried out smoothly at 65 degrees C to give a variety of carbinol derivatives in good to excellent yields using a mixture of [bmim][PF6] and water as the solvent. The isolation of the products was readily performed by the extraction with diethyl ether, and the Pd(OAc)(2)/P(1-Nap)(3)/[bmim][PF6]/H2O system could be easily recycled and reused six times without significant loss of catalytic activity. Our system not only avoids the use of easily volatile THF or toluene as solvent but also solves the basic problem of palladium catalyst and these phosphine ligand reuse. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:50 / 56
页数:7
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