- Chemical Name:Diphenyliodanium;hydrobromide
- CAS No.:1483-73-4
- Molecular Formula:C12H10 I . Br
- Molecular Weight:361.02
- Hs Code.:29319090
- NSC Number:8980
- Mol file:1483-73-4.mol
Synonyms:diphenyliodanium;hydrobromide;SCHEMBL3169505;NSC8980;NSC-8980
Synonyms:diphenyliodanium;hydrobromide;SCHEMBL3169505;NSC8980;NSC-8980
99%, *data from raw suppliers
Diphenyliodonium Bromide *data from reagent suppliers
There total 9 articles about Diphenyliodanium;hydrobromide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:
Reference yield: 95.0%
Reference yield: 92.0%
Reference yield: 77.0%
The research explores the synthesis of N-phenyl methyl esters of various amino acids using diphenyliodonium bromide as a key reagent. The study focuses on the efficient and selective N-phenylation of α-amino acids, including glycine, alanine, valine, leucine, isoleucine, phenylalanine, methionine, proline, serine, threonine, tyrosine, aspartic acid, and glutamic acid. The process involves converting the amino acids into their methyl ester hydrochloride salts, followed by neutralization to obtain free amines. These amines are then subjected to N-phenylation in the presence of diphenyliodonium bromide, silver nitrate, and a catalytic amount of copper bromide. The chiral integrity of the amino acids is maintained throughout the reactions, as confirmed by the synthesis of dipeptides for each N-phenyl amino acid. The structures of the new compounds are characterized using IR, 1H, and 13C NMR spectroscopy, as well as CHN microanalysis or high-resolution mass spectrometry. The study highlights the utility of diphenyliodonium bromide in the synthesis of N-phenylated amino acids, demonstrating good to excellent yields and maintaining the chirality of the starting amino acids.