The preparation of ester heterocycles mostly uses heteroatoms as nucleophilic sites, which are achieved by intramolecular substitution or addition reactions. Compound: 4-(Piperazin-1-yl)phenol( cas:56621-48-8 ) is researched.Computed Properties of C10H14N2O.Nematollahi, Davood; Momeni, Shima; Khazalpour, Sadegh published the article 《Different strategies in electrochemical synthesis of new mono and di-substituted hydroquinone and benzoquinone》 about this compound( cas:56621-48-8 ) in Electrochimica Acta. Keywords: strategy electrochem synthesis mono di hydroquinone benzoquinone derivative. Let’s learn more about this compound (cas:56621-48-8).
Electrochem. syntheses of 2-indolyl-5-arylsulfonyl-p-benzoquinone derivatives were carried out in two successive oxidation steps. The 1st involves the oxidation of hydroquinone, 4-(piperazin-1-yl)-phenol and 1-(4-(4-hydroxyphenyl)-piperazin-1-yl) ethanone in the presence of arylsulfinic acids as nucleophiles. The authors’ voltammetric data indicate that electrochem. generated p-benzoquinone participates in Michael addition reaction with arylsulfinic acids leading to the 2-(arylsulfonyl) benzene-1,4-diols. The 2nd consists of the oxidation of 2-(arylsulfonyl) benzene-1,4-diols in the presence of 1,2-dimethylindole and the formation of 2-indolyl-5-arylsulfonyl-p-benzoquinone derivatives as the final products. A plausible mechanism for the synthesis of 2-indolyl-5-arylsulfonyl-p-benzoquinone derivatives is also presented.
There is still a lot of research devoted to this compound(SMILES：OC1=CC=C(N2CCNCC2)C=C1)Computed Properties of C10H14N2O, and with the development of science, more effects of this compound(56621-48-8) can be discovered.
Reference:
Ether – Wikipedia,
Ether | (C2H5)2O – PubChem