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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 436199Generated: October 30, 2026

Iodoethane → 2-(3-Ethoxyphenyl)-5H-[1,2,4]triazolo[5,1-a]isoindole

https://huagongshe.com/reaction/436199

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantSodium ethoxideHCID 2723922—
ReactantHCID 21455283HCID 21455283—
SolventEthanolHCID 702—
Product2-(3-Ethoxyphenyl)-5H-[1,2,4]triazolo[5,1-a]isoindoleHCID 13445173%

Reaction Steps

2-(3-Hydroxyphenyl)-5H-s-triazolo[5,1-a] isoindole (1.25 g, 0.05 mole) is added to 20 ml of ethanol containing one equivalent proportion of sodium ethoxide. To this mixture is added 0.49 ml (0.06 mole) of ethyl iodide in 5 ml of ethanol. After stirring for one hour at room temperature, a further amount of 0.49 ml of ethyl iodide is added. After refluxing for one hour the solvent is distilled off and the residue is washed with water and extracted with dichloromethane. Evaporation of the solvent and crystallization of the residue from ethanol gives 1 g (73%) of the title product, m.p. 166°-7° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04007276
Source datasetuspto-grants-1977_02
ORD IDord-410221a369704c02b3a1f49c9d41d587
Source noteuspto-grants-1977_02