TY - JOUR
T1 - Green synthesis of 5-substituted-1H-1,2,3,4-tetrazoles and 1-sustituted-1H-1,2,3,4-tetrazoles via [3+2] cycloaddition by reusable immobilized AlCl3on ã-Al2O3
AU - Nanjundaswamy, Hemmaragala Marishetty
AU - Abrahamse, Heidi
N1 - Publisher Copyright:
© 2014 The Japan Institute of Heterocyclic Chemistry.
PY - 2014
Y1 - 2014
N2 - We report the effectiveness of the surface modified γ-Al2O3which is reusable, efficient, catalytic, safe and environmentally acceptable procedure for the conversion of both alkyl and aryl nitriles into the corresponding 5-substituted-1H-1,2,3,4-tetrazoles via [3+2] cycloaddition with sodium azide in excellent yields at mild reaction conditions (50 ° C). The catalyst also afforded 1-substituted-1H-1,2,3,4-tetrazoles by the reaction of amines, sodium azide and triethyl orthoformate. The catalyst could be recycled and was reused eleven runs without losing its activity.
AB - We report the effectiveness of the surface modified γ-Al2O3which is reusable, efficient, catalytic, safe and environmentally acceptable procedure for the conversion of both alkyl and aryl nitriles into the corresponding 5-substituted-1H-1,2,3,4-tetrazoles via [3+2] cycloaddition with sodium azide in excellent yields at mild reaction conditions (50 ° C). The catalyst also afforded 1-substituted-1H-1,2,3,4-tetrazoles by the reaction of amines, sodium azide and triethyl orthoformate. The catalyst could be recycled and was reused eleven runs without losing its activity.
UR - http://www.scopus.com/inward/record.url?scp=84907015367&partnerID=8YFLogxK
U2 - 10.3987/COM-14-13048
DO - 10.3987/COM-14-13048
M3 - Article
AN - SCOPUS:84907015367
SN - 0385-5414
VL - 89
SP - 2137
EP - 2150
JO - Heterocycles
JF - Heterocycles
IS - 9
ER -