15517-46-1Relevant articles and documents
1. 4 - b (4 - hydroxybenzene acyl) rectifying section polyetherketoneetherketoneketone copolymer preparation method
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Paragraph 0024-0025, (2017/08/25)
The invention relates to a 1,4-dis(4-hydroxyl pyrazolyl)benzene and a preparation method of a polyetheretherketone copolymer, which belongs to the high-molecular material field. The method comprises the following steps: selecting nitrobenzene and tetrachloroethanes as solvents, taking aluminium trichloride as a catalyst for a Fries rearrangement reaction to obtain a 1,4-dis(4-hydroxyl pyrazolyl)benzene monomer, then adding 4,4'-difluorobenzophenone and sulfobenzide in a reaction container equipped with a thermometer, protecting under nitrogen, heating to 160-180 DEG C and adding carbonate, heating to 165-190 DEG C and adding a bisphenol monomer, wherein the bisphenol monomer is a mixture of hydroquinone and 1,4-dis(4-hydroxyl pyrazolyl)benzene, performing a program temperature control reaction to obtain a polymer, and processing to obtain the refined polyetheretherketone random polymer.
Visible Light Copper Photoredox-Catalyzed Aerobic Oxidative Coupling of Phenols and Terminal Alkynes: Regioselective Synthesis of Functionalized Ketones via C C Triple Bond Cleavage
Sagadevan, Arunachalam,Charpe, Vaibhav Pramod,Ragupathi, Ayyakkannu,Hwang, Kuo Chu
supporting information, p. 2896 - 2899 (2017/03/11)
Direct oxidative coupling of phenols and terminal alkynes was achieved at room temperature by a visible-light-mediated copper-catalyzed photoredox process. This method allows regioselective synthesis of hydroxyl-functionalized aryl and alkyl ketones from simple phenols and phenylacetylene via C C triple bond cleavage. 47 examples were presented. From a synthetic perspective, this protocol offers an efficient synthetic route for the preparation of pharmaceutical drugs, such as pitofenone and fenofibrate.