Duesel, Simon Josef Siegfried; Koenig, Burkhard published an article in 2020, the title of the article was Oxidative Photochlorination of Electron-Rich Arenes via in situ Bromination.Recommanded Product: 2-Methoxynaphthalene And the article contains the following content:
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 byproducts. The experimental process involved the reaction of 2-Methoxynaphthalene(cas: 93-04-9).Recommanded Product: 2-Methoxynaphthalene
The Article related to chloroarene regioselective preparation, arene oxidative photochlorination photoredox catalyst, Benzene, Its Derivatives, and Condensed Benzenoid Compounds: Halides and Halonium Compounds and other aspects.Recommanded Product: 2-Methoxynaphthalene
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