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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856134Generated: October 29, 2026

Sodium Iodide → 5-(2-methyloxiran-2-ylmethylthio)-1-phenyl-1H-tetrazole

https://huagongshe.com/reaction/856134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Methyloxiran-2-ylmethyl paratoluenesulfonateHCID 14237194—
Reactant1-phenyltetrazole-5-thiolHCID 178527986—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-(2-methyloxiran-2-ylmethylthio)-1-phenyl-1H-tetrazoleHCID 2308153439%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-phenyl-5-mercapto-1H-tetrazole (3.5 g, 19.64 mmol), (2-methyl-2-oxiranylmethyl) toluene-4-sulfonate (5 g, 20.64 mmol), potassium carbonate (3 g, 21.71 mmol), and sodium iodide (4.5 g, 30.02 mmol) in DMF (30 ml) was stirred at 60° C. for 6 hours. The reaction mixture was was poured into water, and extracted with ethyl acetate twice. The extracts were combined, washed with 5% sodium hydroxide aqueous solution and then with water three times, and dried over sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1) to afford 5-(2-methyl-2-oxiranylmethylsulfanyl)-1-phenyl-1H-tetrazole (1.9 g, yield 39%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-2a3832d3910c437199b83a667faa9980
Source noteuspto-grants-2007_08