《Transition-Metal-Free Borylation of Aryl Bromide Using a Simple Diboron Source》 was published in Journal of Organic Chemistry in 2020. These research results belong to Lim, Taeho; Ryoo, Jeong Yup; Han, Min Su. COA of Formula: C7H7BrO The article mentions the following:
The authors developed a simple and atom-economic transition-metal-free borylation reaction of aryl bromides. An atom-economic and com. available diboron source, bis-boronic acid (BBA), was used, and the borylation reaction was performed using a simple procedure at a mild temperature Under mild conditions, aryl bromides were converted to arylboronic acids directly without any deprotection steps, and the functional group tolerance was considerably high. The mechanism study suggested that this borylation reaction proceeds via a radical pathway. This simple borylation reaction will be useful for the synthesis of valuable arylboronic acids. The experimental process involved the reaction of 1-Bromo-3-methoxybenzene(cas: 2398-37-0COA of Formula: C7H7BrO)
1-Bromo-3-methoxybenzene(cas: 2398-37-0) is a compound useful in organic synthesis and other chemical processes. It is an intermediate used for pharmaceuticals, perfumes and agrochemicals.COA of Formula: C7H7BrO
Referemce:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem