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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1073787Generated: November 1, 2026

1-Bromohexane → Sbb043676

https://huagongshe.com/reaction/1073787

Reaction equation

Participants

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

Reaction Steps

In 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 solution, 99 g of 1-bromohexane was added and the resulting mixture was warmed to 60°~70° C. and stirred for 2 hours. After cooling, water was added to the reaction mixture, and the resulting solution was filtered. The residue was washed with water and dried under reduced pressure. The dried residue was recrystallized from an ethanol/hexane mixture, and 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 numberUS04971971
Source datasetuspto-grants-1990_11
ORD IDord-5267acc46329413ca55d2359d49b20ee
Source noteuspto-grants-1990_11