520-79-6Relevant academic research and scientific papers
A convenient and efficient H2SO4-promoted regioselective monobromination of phenol derivatives using N-bromosuccinimide
Wu, Yong-Qi,Lu, Hai-Jia,Zhao, Wen-Ting,Zhao, Hong-Yi,Lin, Zi-Yun,Zhang, Dong-Feng,Huang, Hai-Hong
supporting information, p. 813 - 822 (2020/02/15)
A convenient, rapid H2SO4-promoted regioselective monobromination reaction with N-bromosuccinimide was developed. The desired para-monobrominated or ortho-monobrominated products of phenol derivatives were obtained in good to excellent yields with high selectivity. Regioselective chlorination and iodination were also achieved in the presence of H2SO4 using N-chlorosuccinimide and N-iodosuccinimide, respectively.
Electrophilic Catalysis of Sulphate (-SO3-) Group Transfer: Hydrolysis of Salicyl Sulphates assisted by Intramolecular Hydrogen Bonding
Hopkins, Andrew Ramsay,Green, Adam Llywellyn,Williams, Andrew
, p. 1279 - 1284 (2007/10/02)
The hydrolysis of substituted salicyl sulphates has been measured over a range of pH values at 70 deg C to obtain kinetic parameters for hydronium ion (kH) and carboxylic acid (kp) calalysis.A Jaffe treatment of the carboxy-catalysis parameter for a range of nuclear substituents yields ρphenol 1.51; ρcarboxy 0 indicates that the carboxy-function does not ionise on going from the ground- to the transition-state, consistent with hydrogen bonding rather than catalysis through proton transfer.The change in 'effective' charge on the phenol oxygen on going from the ground- to the transition-state confirms less build up of negative charge than in the uncatalysed hydrolysis of aryl sulphates.
