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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 982211Generated: October 30, 2026

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

https://huagongshe.com/reaction/982211

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 magenesium 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 numberUS04994479
Source datasetuspto-grants-1991_02
ORD IDord-c5ce11a7943041afa74527a3b7a73fe6
Source noteuspto-grants-1991_02