Simple and Clean Photo-induced Methylation of Heteroarenes with MeOH

被引:171
作者
Liu, Wenbo [1 ,2 ]
Yang, Xiaobo [1 ,2 ]
Zhou, Zhong-Zhen [1 ,2 ]
Li, Chao-Jun [1 ,2 ]
机构
[1] McGill Univ, Dept Chem, 801 Sherbrooke St West, Montreal, PQ H3A 0B8, Canada
[2] McGill Univ, FQRNT Ctr Green Chem & Catalysis, 801 Sherbrooke St West, Montreal, PQ H3A 0B8, Canada
来源
CHEM | 2017年 / 2卷 / 05期
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
C-H BONDS; PALLADIUM-CATALYZED METHYLATION; HETEROAROMATIC BASES; NUCLEOPHILIC CHARACTER; SELECTIVE ALKYLATION; CARBONYL-COMPOUNDS; CARBOXYLIC-ACIDS; PHOTOCHEMISTRY; FUNCTIONALIZATION; HETEROCYCLES;
D O I
10.1016/j.chempr.2017.03.009
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Heteroarene methylation utilizing a cheap and safe methylation source without involving transition metals represents an important yet challenging objective. Here, a simple and clean catalyst-free protocol for the methylation of various heteroarenes (including six-and five-membered types) is described under light irradiation. This protocol employs cheap, readily available, and abundant MeOH as both the solvent and the methylation source. It was found that adding dichloromethane (DCM) as a co-solvent could significantly increase the yield of the methylation products. Heteroarenes bearing various functional groups could be methylated and tri-deuteromethylated successfully. Deuterium labeling studies suggested that the newly generated methyl group in the products consisted of two hydrogens from the methyl group and one hydrogen from the OH group in MeOH.
引用
收藏
页码:688 / 702
页数:15
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