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TAIW
ORGANIC PROCESS RESEARCH & DEVELOPMENT · 2014 · IF 2.549

Synthesis of 2,6,8,12-Tetraacetyl-2,4,6,8,10,12-hexaazaisowurtzitane (TAIW) from 2,6,8,12-Tetraacetyl-4,10-dibenzyl-2,4,6,8,10,12-hexaazaisowurtzitane (TADBIW) by Catalytic Hydrogenolysis Using a Continuous Flow Process

Kai Dong,Cheng H. Sun,Jian W. Song,Gai X. Wei,Si P. Pang

Synthesis of 2,6,8,12-tetraacetyl-2,4,6,8,10,12-hexaazaisowurtzitane (TAIW) by catalytic hydrogenolysis of 2,6,8,12-tetraacetyl-4,10-dibenzyl-2,4,6,8,10,12-hexaazaisowurtzitane (TADBIW), a key step for the synthesis of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (HNIW), has been first implemented under continuous flow conditions using the commercially available H-Cube Pro reactor. Several variables (i.e., reaction temperature, flow rate, and pressure) and the stability of the system have been investigated to optimize the operating conditions. The results show that a continuous flow system provides a better yield than a batch system. For instance, the yield is 99% at the optimized conditions, while the best yield from batch reactions is 92%. Continuous flow synthesis of TAIW has potential applications in improving the production technologies of HNIW for its many advantages over batch reactions.

CAS / MDL: 64-19-7
研究领域: 化学合成 · 材料科学
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INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2025 · IF 3.9

A Simple Method to Prepare the High Performance Pd(OH)2/C for C–N Bond Cleavage

Bin Zhang,Xiaodong Guo,Xin Feng,Xiaoxia Duan,Guilong Wang,Chao Yang

The debenzylation reaction of hexabenzylhexaazaisowurtzitane (HBIW) and 2,6,8,12-tetraacetyl-4,10-dibenzyl-2,4,6,8,10,12-hexaazaisowurtzitane (TADBIW) to synthesize 2,6,8,12-tetraacetyl-2,4,6,8,10,12-hexaazaisowurtzitane (TAIW) is the major challenge in the production of 2,4,6,8,10,12-hexanitro-2,4,6,8,10,12-hexaazaisowurtzitane (HNIW). This is primarily attributed to the reaction needing a lot of palladium catalysts, which tend to deactivate rapidly during the process. In this work, a series of Pd(OH)2/C catalysts were successfully prepared through a convenient deposition-precipitation method by controlling the flow rate of the PdCl2 solution. Employing the 10% Pd(OH)2/C–F0.5 sample, the debenzylation reaction was successfully completed with a lower usage of Pd and shorter time of reaction. For the HBIW debenzylation reaction, the yield of TADBIW was 87.4% at low temperature (25 °C) when 1‰ Pd/HBIW was used, and the higher yield was 89.8% at high temperature (45 °C) when 3‰ Pd/HBIW was used. The TADBIW/Pd/h values of them were 42.5 and 95.7, respectively. For the TADBIW debenzylation reaction, the complete conversion of the reactant was realized when Pd/TADBIW was 2‰. The value of TAIW/Pd/h was 154.6 when Pd/TADBIW was 4‰, which was higher than the reports. Compared to the reported catalysts, the dosage of Pd used in the debenzylation reactions of HBIW and TADBIW was significantly decreased. Furthermore, the 10% Pd(OH)2/C–F0.5 sample was recycled six times with similar performance, demonstrating excellent stability. Based on the analysis of characterization results, it is effortless to find that the flow rate of the PdCl2 solution plays a key role in controlling the adsorption behavior of palladium species on activated carbon. The lower flow rate is beneficial to obtaining Pd nanoparticles with a smaller size, a higher proportion of Pd2+, and a higher metal distribution. This study may provide a simple way to develop palladium catalysts with high performance for related applications.

CAS / MDL: 108-86-1 127-19-5
研究领域: 化学工程 · 催化材料科学
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