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. 2015 Dec 3;6:2300–2309. doi: 10.3762/bjnano.6.236

Table 2.

Preparation of 1-substituted 1H-1,2,3,4-tetrazoles in the presence of Cu NPs/bentonite by reaction between sodium azide, primary amines and triethyl orthoformate at 120 °C.a

Entry Substrate Product Yield [%]b

1 graphic file with name Beilstein_J_Nanotechnol-06-2300-i001.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i002.jpg 93
2 graphic file with name Beilstein_J_Nanotechnol-06-2300-i003.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i004.jpg 85
3 graphic file with name Beilstein_J_Nanotechnol-06-2300-i005.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i006.jpg 94
4 graphic file with name Beilstein_J_Nanotechnol-06-2300-i007.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i008.jpg 87
5 graphic file with name Beilstein_J_Nanotechnol-06-2300-i009.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i010.jpg 83
6 graphic file with name Beilstein_J_Nanotechnol-06-2300-i011.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i012.jpg 85
7 graphic file with name Beilstein_J_Nanotechnol-06-2300-i013.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i014.jpg 87
8 graphic file with name Beilstein_J_Nanotechnol-06-2300-i015.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i016.jpg 87
9 graphic file with name Beilstein_J_Nanotechnol-06-2300-i017.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i018.jpg 88
10 graphic file with name Beilstein_J_Nanotechnol-06-2300-i019.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i020.jpg 92
11 graphic file with name Beilstein_J_Nanotechnol-06-2300-i021.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i022.jpg 86
12 graphic file with name Beilstein_J_Nanotechnol-06-2300-i023.jpg graphic file with name Beilstein_J_Nanotechnol-06-2300-i024.jpg 83

aReaction conditions: Amine (2.0 mmol), NaN3 (2 mmol), triethyl orthoformate (2.4 mmol), Cu NPs/bentonite (0.05 g) at 120 °C, 3 h. bIsolated yield.