《Trichloroacetimidate-Triggered Expeditious and Novel Synthesis of N-Acylbenzotriazoles》 was written by Yadav, Mangal S.; Jaiswal, Manoj K.; Kumar, Sunil; Tiwari, Vinod K.. Synthetic Route of C7H5IO2 And the article was included in SynOpen in 2021. The article conveys some information:
A facile route for the synthesis of a diverse range of N-acylbenzotriazole derivatives from the corresponding carboxylic acids has been established through a carbonyl activation pathway. In this method, trichloroacetonitrile is performed as an effective reagent for an easy access of N-acylbenzotriazoles which was simply proceeded through the activation of carboxylic acids via in situ imidate formation in anhydrous 1,2-dichloroethane followed by addition of 1H-benzotriazole at 80° for 3-4 h. Easy handling, one-pot, and metal-free conditions demonstrate the notable merits of the devised protocol. The results came from multiple reactions, including the reaction of 2-Iodobenzoic acid(cas: 88-67-5Synthetic Route of C7H5IO2)
2-Iodobenzoic acid(cas: 88-67-5) belongs to organic iodides. The carbon-iodine bond is weaker than other carbon-halogen bonds due to the poor electronegative nature of the iodine atom. Synthetic Route of C7H5IO2 Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond.
Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com