2150-95-0Relevant academic research and scientific papers
Reductive acylation of nitroarenes to anilides by sodium sulfite in carboxylic acids
Ghaffarzadeh, Mohammad,Akhavan, Pegah
supporting information, p. 1417 - 1419 (2016/09/28)
A facile and efficient reductive acylation of aromatic nitro compounds to corresponding anilides using a sodium sulfite-carboxylic acid system for the first time has been reported. The sodium sulfite reagent provides the colorless reductant in combination with stoichiometric amounts of carboxylic acid and enables the formation of anilides from nitroarenes without any additives in good to excellent yields with high purities and simple work-up. Furthermore, this protocol provides a novel and complementary access to some industrially important chemicals in kilogram scale under mild conditions.
A novel synthesis of N-arylamides from nitroarenes via reductive N-acylation with red phosphorus and iodine
Du, Xiaohua,Zheng, Mei,Chen, Sheng,Xu, Zhenyuan
, p. 1953 - 1955 (2008/02/08)
A series of N-arylamides and imides were synthesized via reductive N-acylation of nitroarenes with red phosphorus and carboxylic acids, catalyzed by iodine or iodides; an I /I° redox cycle was proposed to promote the reaction. Georg Thieme Verlag Stuttgart.
