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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 847272Generated: October 30, 2026

Ethanol → Ethyl 2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]acetate

https://huagongshe.com/reaction/847272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl bromoacetateHCID 7748—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178509208HCID 178509208—
SolventWaterHCID 962—
ProductEthyl 2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]acetateHCID 35191242.1%

Reaction Steps

To a mixture of 3.9 g of 2-amino-5-mercapto-1,3,4-thiadiazole, 4.2 g of potassium carbonate and 50 ml of ethanol was gradually added 5 g of ethyl bromoacetate under ice cooling. Then, the mixture was stirred at room temperature for 3 hours. To the reaction mixture was added 200 ml of water followed by extraction with ethyl acetate. After washing with water, the extract was dried over anhydrous magnesium sulfate and the solvent was distilled off. The solid obtained was washed with toluene and dried to obtain 2.7 g of ethyl [(5-amino-1,3,4-thiadiazol-2-yl)thio]acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05140046
Source datasetuspto-grants-1992_08
ORD IDord-85c6056e5d4c418fa65e18386d6d89b0
Source noteuspto-grants-1992_08