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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733131Generated: November 1, 2026

Iodoethane → L 11204

https://huagongshe.com/reaction/1733131

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
Reactant3-(5,6-Dihydro[1,2,4]triazolo[5,1-a]isoquinolin-2-yl)phenolHCID 134401—
ReactantSodium ethoxideHCID 2723922—
SolventEthanolHCID 702—
ProductL 11204HCID 119282—

Reaction Steps

2-(3-Hydroxyphenyl)-5,6-dihydro-s-triazolo-[5,1-a]isoquinoline (3.95 g.) is added to 60 ml. of ethanol containing one equivalent proportion of sodium ethoxide. To this mixture is added 1.57 ml. of ethyl iodide in 15 ml. of ethanol. After stirring for one hour at room temperature, a further 1.57 ml. of ethyl iodide is added and the mixture is refluxed for 18 hours. 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 3.87 g. of the title product; m.p. 102°-3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE030456
Source datasetuspto-grants-1980_12
ORD IDord-002d50ccb2624136b497e578878b5b7b
Source noteuspto-grants-1980_12