In 2019,Green Chemistry included an article by Ke, Fang; Xu, Yiwen; Zhu, Suning; Lin, Xiaoyan; Lin, Chen; Zhou, Sunying; Su, Huimin. Related Products of 88-67-5. The article was titled 《Electrochemical N-acylation synthesis of amides under aqueous conditions》. The information in the text is summarized as follows:
An electrochem. N-acylation of carboxylic acids with amines was reported for the synthesis of amides I [R1 = H, 4-CN, 2-I, etc.; R2 = H, 4-Me, 4-Cl, etc.]. The sustainable TBAB electrocatalysis proceeded with excellent chemoselectivity and positional selectivity, and with ample scope, allowing electrochem. N-acylation under mild reaction conditions at room temperature in water. Moreover, the synthetic utility of the current method was demonstrated by the synthesis of melatonin. In the experimental materials used by the author, we found 2-Iodobenzoic acid(cas: 88-67-5Related Products of 88-67-5)
2-Iodobenzoic acid(cas: 88-67-5) belongs to organic iodides. Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond.Related Products of 88-67-5Iodo alkanes participate in a variety of organic synthesis reactions, which include the SimmonsSmith reaction (cyclopropanation using iodomethane), Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction.
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com