Acid-catalyzed chemodivergent reactions of 2,2-dimethoxyacetaldehyde and anilines

被引:4
作者
Guo, Luxia [1 ]
Chen, Zihao [1 ]
Zhu, Hongmei [1 ]
Li, Minghao [1 ]
Gu, Yanlong [1 ,2 ,3 ]
机构
[1] Huazhong Univ Sci & Technol, Hubei Key Lab Mat Chem & Serv Failure, Wuhan 430074, Peoples R China
[2] Lanzhou Inst Chem Phys, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Peoples R China
[3] Shihezi Univ, Key Lab Green Proc Chem Engn Xinjiang Bingtuan, Shihezi 832004, Peoples R China
基金
中国国家自然科学基金;
关键词
Condition-determined reaction; Chemodivergent reaction; 2,2-Dimethoxyacetaldehyde; C-C bond cleavage; Heyns rearrangement; C BOND-CLEAVAGE; ALDEHYDES; KETONES; REARRANGEMENT; ACCESS;
D O I
10.1016/j.cclet.2020.10.033
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chemodivergent reactions of 2,2-dimethoxyacetaldehyde and anilines were described, which were established on the basis of either a C-C bond cleavage or a rearrangement process of a reaction intermediate. These reactions proceeded in a condition-determined manner with good functional group tolerance. In the first model, 2,2-dimethoxyacetaldehyde reacted with aniline to form a new C-N bond, in the presence of O-2, via a C-C bond cleavage reaction. However, in the second model, by performing the reaction in the absence of O-2, Heyns rearrangement occurred and generated a new C-O bond to form methyl phenylglycinate. Such condition-determined reactions not only offered the new way for value-added conversion of biomass-derived platform molecule, 2, 2-dimethoxyacetaldehyde, but also provided efficient methods for the synthesis of N-arylformamides and methyl phenylglycinates. (C) 2020 Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1419 / 1422
页数:4
相关论文
共 39 条
[31]   SELECTIVITY - A KEY TO SYNTHETIC EFFICIENCY [J].
TROST, BM .
SCIENCE, 1983, 219 (4582) :245-250
[32]   Chemodivergent Tandem Cyclizations of 2-Indolylmethanols with Tryptophols: C-N versus C-C Bond Formation [J].
Wang, Jing-Yi ;
Wu, Ping ;
Wu, Jia-Le ;
Mei, Guang Jian ;
Shi, Feng .
JOURNAL OF ORGANIC CHEMISTRY, 2018, 83 (11) :5931-5946
[33]   A Convenient Method for Cleavage of Amide C-N Bond [J].
Wei, Yingfei ;
Shi, Daxing ;
Wei, Zhen ;
Xu, Juan ;
Li, Jiarong .
CHINESE JOURNAL OF ORGANIC CHEMISTRY, 2012, 32 (06) :1126-1130
[34]   W Iron-catalyzed aerobic oxidative cleavage of the C-C σ-bond using air as the oxidant: chemoselective synthesis of carbon chain-shortened aldehydes, ketones and 1,2-dicarbonyl compounds [J].
Xing, Qi ;
Lv, Hui ;
Xia, Chungu ;
Li, Fuwei .
CHEMICAL COMMUNICATIONS, 2016, 52 (03) :489-492
[35]   Catalyst-Controlled Chemodivergent Modification of Indoles with 2-Furylcarbinols: Piancatelli Reaction vs Cross-Dehydrative Coupling Reaction [J].
Xu, Jianfeng ;
Luo, Yi ;
Xu, Huaping ;
Chen, Zhengkai ;
Miao, Maozhong ;
Ren, Hongjun .
JOURNAL OF ORGANIC CHEMISTRY, 2017, 82 (07) :3561-3570
[36]   Bronsted acid-catalyzed facile synthesis of α-substituted N-arylaminoacetals and their downstream conversions to functionalized pyrroles [J].
Yang, Jian ;
Wang, Xin ;
El-Harairy, Ahmed ;
Bai, Rongxian ;
Gu, Yanlong .
MOLECULAR CATALYSIS, 2019, 468 :36-43
[37]   Cleavage of the C-C triple bond of ketoalkynes: synthesis of 4(3H)-quinazolinones [J].
Yang, Xifa ;
Cheng, Guolin ;
Shen, Jinhai ;
Kuai, Changsheng ;
Cui, Xiuling .
ORGANIC CHEMISTRY FRONTIERS, 2015, 2 (04) :366-368
[38]   Intermediate-Dependent Unusual [4+3], [3+2] and Cascade Reactions of 3-Indolylmethanols: Controllable Chemodivergent and Stereoselective Synthesis of Diverse Indole Derivatives [J].
Zhang, Hong-Hao ;
Zhu, Zi-Qi ;
Fan, Tao ;
Liang, Jing ;
Shi, Feng .
ADVANCED SYNTHESIS & CATALYSIS, 2016, 358 (08) :1259-1288
[39]   Chemodivergent Couplings of N-Arylureas and Methyleneoxetanones via Rh(III)-Catalyzed and Solvent-Controlled C-H Activation [J].
Zhu, Guoxun ;
Shi, Wendi ;
Gao, Hui ;
Zhou, Zhi ;
Song, Huacan ;
Yi, Wei .
ORGANIC LETTERS, 2019, 21 (11) :4143-4147