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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252095Generated: November 2, 2026

Ethanol → Sbb043676

https://huagongshe.com/reaction/1252095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1-BromohexaneHCID 8101—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178509208HCID 178509208—
SolventWaterHCID 962—
ProductSbb043676HCID 157947277.1%

Reaction Steps

To 190 ml of ethanol and 240 ml of water, 81.5 g of 2-amino-5-mercapto-1,3,4-thiadiazole and 26.9 g of sodium hydroxide were added. To this mixture 99.0 g of 1-bromohexane was added and the resulting mixture was stirred at 60°-70° C. for 2 hours. After cooling, water was added to the mixture and the mixture was filtered. The residue was washed with water, dried under reduced pressure, and recrystallized from an ethanol/hexane mixture. Thus 100.5 g of 2-amino-5-hexylthio-1,3,4-thiadiazole was obtained. m.p. 113°-115° C. Yield 77%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04742063
Source datasetuspto-grants-1988_05
ORD IDord-5c2db0debd1f48c0a317cc74015b94a9
Source noteuspto-grants-1988_05