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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1758325Generated: November 3, 2026

Potassium Iodide → 1-Methyl-5-[3-(3-hydroxy-2-pyridyl)thiopropyl]thio-1,2,3,4-tetrazole

https://huagongshe.com/reaction/1758325

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant1-Methyl-5-(3-chloropropyl)thio-1,2,3,4-tetrazoleHCID 12803376—
ReactantHCID 178516238HCID 178516238—
SolventAcetoneHCID 180—
Product1-Methyl-5-[3-(3-hydroxy-2-pyridyl)thiopropyl]thio-1,2,3,4-tetrazoleHCID 1306194142.9%

Reaction Steps

1-Methyl-5-(3-chloropropyl)thio-1,2,3,4-tetrazole (1.9 g) and 3-hydroxy-2-mercaptopyridine (1.3 g) are dissolved in acetone (50 ml). To the mixture are added potassium carbonate (1.4 g) and potassium iodide (0.1 g), and the mixture is refluxed for 5 hours. After acetone is distilled off, water is added to the residue, and the mixture is extracted with chloroform. The chloroform solution is washed with saturated aqueous sodium chloride and dried over magnesium sulfate. After chloroform is distilled off, the residue is purified by column chromatography (Kieselgel 60), followed by eluting with chloroform-methanol and recrystallizing from ethyl acetate-n-hexane to give 1-methyl-5-[3-(3-hydroxy-2-pyridyl)thiopropyl]thio-1,2,3,4-tetrazole (1.2 g) as pale yellow granules, m.p. 87.5°-88.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04372953
Source datasetuspto-grants-1983_02
ORD IDord-eb0192b257b94d2e9aafeb118d3ce033
Source noteuspto-grants-1983_02