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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252091Generated: October 30, 2026

1-Bromohexane → Sbb043676

https://huagongshe.com/reaction/1252091

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexaneHCID 8101—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178509208HCID 178509208—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductSbb043676HCID 157947278.7%

Reaction Steps

In 24 ml of water and 24 ml of ethanol, 11.6 g of 2-amino-5-mercapto-1,3,4-thiadiazole and 3.8 g of sodium hydroxide were dissolved, 14.0 g of 1-bromohexane was added to this solution, and the mixture was heated to 70°-80° C. and stirred for 3 hours. After cooling, water was added and the mixture was filtered. The residue was washed with water, dried under reduced pressure, and recrystallized from an ethanol/n-hexane (1:1) mixture. Thus 14.5 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-6432914c090d4f8787e299adb34c0060
Source noteuspto-grants-1988_05