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Bi 2 O 3 /FAp, a sustainable catalyst for synthesis of dihydro‐[1,2,4]triazolo[1,5‐a]pyrimidine derivatives through green strategy
Author(s) -
Kerru Nagaraju,
Gummidi Lalitha,
Maddila Surya Narayana,
Bhaskaruni Sandeep V.H.S.,
Jonnalagadda Sreekantha B.
Publication year - 2020
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.5590
Subject(s) - chemistry , catalysis , bismuth , yield (engineering) , fourier transform infrared spectroscopy , nuclear chemistry , heterogeneous catalysis , ethyl acetoacetate , infrared spectroscopy , organic chemistry , chemical engineering , materials science , engineering , metallurgy
The bismuth loaded on fluorapatite (Bi 2 O 3 /FAp) proved to be an excellent catalyst for the synthesis of novel dihydro‐[1,2,4]triazolo[1,5‐a]pyrimidine derivatives via a three‐component reaction involving the mixture of 1 H ‐1,2,4‐triazol‐5‐amine, ethyl cyanoacetate or ethyl acetoacetate, and different benzaldehydes in ethanol at room temperature. The catalyst material was characterized by X‐ray diffraction, Brunauer–Emmett–Teller surface area analysis, Fourier‐transform infrared, scanning electron microscopy, energy‐dispersive X‐ray spectroscopy, and transmission electron microscopy techniques. The efficacy of Bi 2 O 3 /FAp as a heterogeneous catalyst was evaluated with the loading of different wt% of bismuth on FAp. The 2.5% bismuth on FAp performed extremely well as a catalyst with a high yield of products (92%–96%) in a short reaction time (25–35 min). The catalyst was recovered by simple filtration. It showed undiminished activity up to five runs. Simple work‐up, room temperature reaction, short reaction time, high yields, no column chromatography, and good reusability of catalyst are the merits of the proposed protocol. In addition, this process offers 100% carbon efficiency and 98% atom economy with noteworthy fiscal and environmental benefits.