1958
DOI: 10.1021/ja01548a028
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An Improved Synthesis of 5-Substituted Tetrazoles

Abstract: Vol. 80 0.70 g. was shown by infrared analysis to be the starting alcohol IX.The main fraction from the column was then dissolved in 13 ml. of 5% methanolic potassium hydroxide and boiled under reflux for 3 hours to effect hydrolysis. The solution was Rochester, N. Y.(18) K. Folkers and F. Koniuszy (U. S. Patent 2,370,651, March 6, 1945) give for dihydro-/?-erythroidine hydrobromide, m.p, 231-231.5°, ck25d + 107.5°(in water).

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Cited by 411 publications
(188 citation statements)
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“…The tetrazole 5,5'-(1,4-phenylene)bis-1H-tetrazole (H 2 pbtz), necessary for the preparation of 7, was synthesized from 1,4-dicyanobenzene according to a literature procedure [7]. bistetrazolato ligand is a clean and facile step driven forward by the low solubility of the product.…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The tetrazole 5,5'-(1,4-phenylene)bis-1H-tetrazole (H 2 pbtz), necessary for the preparation of 7, was synthesized from 1,4-dicyanobenzene according to a literature procedure [7]. bistetrazolato ligand is a clean and facile step driven forward by the low solubility of the product.…”
Section: Resultsmentioning
confidence: 99%
“…In this work we describe the synthesis, characterization and X-ray single-crystal structure determination of the new tetranuclear Ni (7) and discuss the structural differences between 3 and 7. The results of temperature-dependent magnetic susceptibility measurements on 4, 5, 6, and 7 are also described.…”
Section: Introductionmentioning
confidence: 99%
“…Conc. HCl (130 mmol) was added dropwise to this solution and stirred without heating for 0.5 h, reflux the reaction mixture for 12-16 h. Now this reaction mixture was added with 30 mL of water and stirred for another 0.5 h. The aqueous layer was separated from the organic layer and added 100 mmol of acetic acid after few minutes till white crystals are formed [29,30]. Yield: 7.…”
Section: Synthesis Of Ligandsmentioning
confidence: 99%
“…The first step involves the formation of aromatic tetrazoles by the reaction of the corresponding palkoxylbenzonitrile with sodium azide 7 . Alkylation reaction with the appropriate alkyl halide furnished the 5-(4-alkoxyphenyl)-2-alkyltetrazole, (L 1 a,b (L 2 a,b,c).…”
Section: Phenyltetrazole Ligandsmentioning
confidence: 99%