An article Oxidative Photochlorination of Electron-Rich Arenes via in situ Bromination WOS:000519315900026 published article about CHLORINATION; CHEMISTRY; CHLORIDE; ALKYNES; SUBSTITUTION; HALOGENATION; ACTIVATION; CATALYSIS; EFFICIENT; ALPHA in [Duesel, Simon Josef Siegfried; Koenig, Burkhard] Univ Regensburg, Inst Organ Chem, Univ Str 31, D-93053 Regensburg, Germany in 2020, Cited 41. The Name is Diphenyl oxide. Through research, I have a further understanding and discovery of 101-84-8. Recommanded Product: Diphenyl oxide
Electron-rich arenes are oxidatively photochlorinated in the presence of catalytic amounts of bromide ions, visible light, and 4CzIPN as organic photoredox catalyst. The substrates are brominated in situ in a first photoredox-catalyzed oxidation step, followed by a photocatalyzed ipso-chlorination, yielding the target compounds in high ortho/para regioselectivity. Dioxygen serves as a green and convenient terminal oxidant. The use of aqueous hydrochloric acid as the chloride source reduces the amount of saline by-products.
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Reference:
Ether – Wikipedia,
,Ether | (C2H5)2O – PubChem