Extracurricular laboratory: Synthetic route of 101-84-8

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An article 3-(Ethoxycarbonyl)-1-(5-methyl-5-(nitrosooxy)hexyl)pyridin-1-ium cation: A green alternative to tert-butyl nitrite for synthesis of nitro-group-containing arenes and drugs at room temperature WOS:000517855700004 published article about IONIC LIQUIDS OILS; ORTHO-NITRATION; STEREOSELECTIVE NITRATION; REGIOSPECIFIC SYNTHESIS; AROMATIC SULFONAMIDES; EFFICIENT SYNTHESIS; IPSO-NITRATION; METAL; NITROOLEFINS; NITROARENES in [Natarajan, Palani] Panjab Univ, Dept Chem, Chandigarh 160014, India; Panjab Univ, Ctr Adv Studies Chem, Chandigarh 160014, India in 2020.0, Cited 67.0. The Name is Diphenyl oxide. Through research, I have a further understanding and discovery of 101-84-8. Quality Control of Diphenyl oxide

Due to their remarkable properties, task-specific ionic liquids have turned out to be progressively popular over the last few years in the field of green organic synthesis. Herein, for the first time, we report that a new task-specific nitrite-based ionic liquid such as 3-(ethoxycarbonyl)-1-(5-methyl-5-(nitrosooxy)hexyl) pyridin-1-ium bis(trifluoromethanesulfonyl)imides (TS-N-IL) derived from biodegradable ethyl nicotinate indeed acted as an efficient and eco-friendly reagent for the synthesis of highly valuable nitroaromatic compounds and drugs including nitroxynil, tolcapone, niclofolan, flutamide, niclosamide and nitrazepam. The bridging of an ionic liquid with nitrite group not only increases the yield and rate of direct C-N bond formation reaction but also allows easy product separation and recyclability of a byproduct. Nonvolatile nature, easy synthesis, merely stoichiometric need and mildness are a portion of the extra focal points of TS-N-IL while contrasted with tert-butyl nitrite an outstanding and highly-flammable reagent utilized largely in organic synthesis. (C) 2019 Elsevier Ltd. All rights reserved.

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Reference:
Ether – Wikipedia,
,Ether | (C2H5)2O – PubChem