Abstract

Catalytic reduction of nitro compounds to the amines is of high importance in modern synthetic chemistry. In this study, an efficient method was developed for the transfer hydrogenation of nitro compounds over a magnetic Pd catalyst by the use of NaBH4 as the hydrogen donor. Full nitrobenzene conversion and high selectivity (>99%) of aniline were produced after 1 h at 60 °C in ethanol. The reductions are successfully carried out in presence of a wide variety of other reducible functional groups in the molecule, except halogen and vinyl substitute nitrobenzene. Kinetic studies indicated the active energy for the transfer hydrogenation of nitrobenzene was 20.93 KJ mol−1. The transfer hydrogenation of nitrobenzene was confirmed to proceed via azobenzene as the intermediate. More importantly, the catalyst was very stable without the loss of its catalytic activity.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.