A concise synthesis of 6,7-dihydro-5H-dibenz[c,e]azepin-5-one was written by Goh, Young-Hyoung;Kim, Guncheol;Kim, Bum Tae;Heo, Jung-Nyoung. And the article was included in Heterocycles in 2010.Application of 61150-57-0 This article mentions the following:
A concise and efficient strategy for the synthesis of dibenz[c,e]azepin-5-ones has been developed. The approach relies on a key transformation involving Suzuki-Miyaura coupling of 2-bromobenzyl azides with 2-(methoxycarbonyl)phenylboronic acid, followed by either a stepwise sequence involving Staudinger reaction and lactam formation or one-pot hydrogenation/base-mediated intramol. lactam formation. In the experiment, the researchers used many compounds, for example, 2-Bromo-4-fluorobenzylbromide (cas: 61150-57-0Application of 61150-57-0).
2-Bromo-4-fluorobenzylbromide (cas: 61150-57-0) belongs to organobromine compounds. Most organobromine compounds, like most organohalide compounds, are relatively nonpolar. Many of the alkyl bromine derivatives are excellent alkylating agents since bromides are good leaving groups. Tribromides, like tetrabutylammonium tribromide, are used as a solid source of bromine. N-bromosuccimide (NBS) is used for the selective bromination of allylic bonds.Application of 61150-57-0
Referemce:
Bromide – Wikipedia,
bromide – Wiktionary