An atom-economical addition of methyl azaarenes with aromatic aldehydes via benzylic C(sp3)-H bond functionalization under solvent- and catalyst-free conditions

被引:0
|
作者
Yennamaneni, Divya Rohini [1 ,2 ]
Amrutham, Vasu [1 ,2 ]
Gajula, Krishna Sai [1 ,2 ]
Banothu, Rammurthy [1 ,2 ]
Boosa, Murali [1 ,2 ]
Nama, Narender [1 ,2 ]
机构
[1] Indian Inst Chem Technol, CSIR, Catalysis & Fine Chem Div, Hyderabad 500007, Telangana, India
[2] Acad Sci & Innovat Res, CSIR HRDC Campus,Sect 19, Ghaziabad 201002, UP, India
来源
BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2020年 / 16卷
关键词
aldehydes; azaarenes; benzylic addition; green chemistry; solvent-free conditions; N-SULFONYL ALDIMINES; C-H; NUCLEOPHILIC-ADDITION; DIRECT ALKENYLATION; QUINOLINE; PYRIDINE; HETEROCYCLES; ARYLATION; NITROGEN;
D O I
10.3762/bjoc.16.259
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A convenient practical approach for the synthesis of 2-(pyridin-2-yl)ethanols by direct benzylic addition of azaarenes and aldehydes under catalyst- and solvent-free conditions is reported. This reaction is metal-free, green, and was carried out in a facile operative environment without using any hazardous transition metal catalysts or any other coupling reagents. Different aromatic aldehydes and azaarenes were monitored, and the yields of the resulting products were moderate to excellent. We accomplished several azaarene derivatives under neat conditions through a highly atom-economical pathway. To evaluate the preparative potential of this process, gram-scale reactions were performed up to a 10 g scale.
引用
收藏
页码:3093 / 3103
页数:11
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