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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646500Generated: October 31, 2026

Potassium Iodide → Ethyl [[5-[(4-acetyl-3-hydroxy-2-propylbenzyl)thio]-1,3,4-thiadiazol-2-yl]thio]acetate

https://huagongshe.com/reaction/1646500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Acetyl-3-hydroxy-2-propylbenzyl chlorideHCID 13781022—
ReactantHCID 178473173HCID 178473173—
CatalystTetrabutylammonium BromideHCID 74236—
SolventTolueneHCID 1140—
SolventMethyl Ethyl KetoneHCID 6569—
ProductEthyl [[5-[(4-acetyl-3-hydroxy-2-propylbenzyl)thio]-1,3,4-thiadiazol-2-yl]thio]acetateHCID 1405312694.9%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a mixture of 0.42 g of 4-acetyl-3-hydroxy-2-propylbenzyl chloride, 0.54 g of ethyl [(5-mercapto-1,3,4-thiadiazol-2-yl)thio]acetate, 0.30 g of anhydrous potassium carbonate and 5 ml of methyl ethyl ketone were added catalytic amounts of potassium iodide and tetra-n-butylammonium bromide followed by stirring at 60° C. for 3 hours. The reaction mixture was diluted with toluene and insoluble matters were filtered off. The filtrate was washed with an aqueous sodium hydroxide solution and dried over anhydrous magnesium sulfate. The solvent was then distilled off. The residue was subjected to silica gel column chromatography. Elution with a mixture of hexane-ethyl acetate (5:1) gave 0.75 g of oily ethyl [[5-[(4-acetyl-3-hydroxy-2-propylbenzyl)thio]1,3,4-thiadiazol-2-yl]thio]acetate. Nuclear magnetic resonance spectrum (in CDCl3,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180730
Source datasetuspto-grants-1993_01
ORD IDord-512bdafb4884484d9bc56bd22b30d34d
Source noteuspto-grants-1993_01