π-Delocalization in phosphaphthalimide and its ambident reactivity (O/P) toward main-group electrophiles was written by Shen, Qi;Xu, Jiashi;Chen, Xiaodan. And the article was included in Dalton Transactions in 2022.Synthetic Route of C19H15Cl This article mentions the following:
The report on phosphaphthalimide (1), the P analog of the phthalimide anion, dates back to forty years ago. However, the presence of π-delocalization between two-coordinated P center and neighboring carbonyl groups in 1 was underestimated. Herein, Na salts of 1 were obtained through a convenient procedure on a relatively large scale with a modified procedure. Reactivity studies demonstrated that 1 is indeed a good electrophile and the essential role of π-delocalization in 1 controlling its ambident properties. NBO anal. revealed the p-π conjugation and p-σ* hyperconjugation in 1 affecting its bond lengths in opposite ways. In the experiment, the researchers used many compounds, for example, (Chloromethanetriyl)tribenzene (cas: 76-83-5Synthetic Route of C19H15Cl).
(Chloromethanetriyl)tribenzene (cas: 76-83-5) belongs to organic chlorides. Chlorinated organic compounds are found in nearly every class of biomolecules and natural products including alkaloids, terpenes, amino acids, flavonoids, steroids, and fatty acids. Alkyl chlorides are versatile building blocks in organic chemistry. While alkyl bromides and iodides are more reactive, alkyl chlorides tend to be less expensive and more readily available.Synthetic Route of C19H15Cl
Referemce:
Chloride – Wikipedia,
Chlorides – an overview | ScienceDirect Topics