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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855697Generated: October 30, 2026

1-Bromohexane → HCID 13710783, compound

https://huagongshe.com/reaction/1855697

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromohexaneHCID 8101—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 178418558HCID 178418558—
SolventIsopropanolHCID 3776—
ProductHCID 13710783HCID 1371078370%

Reaction Steps

2,5-bis(n-hexylthio)-1,3,4-thiadiazole was prepared in over 70% yield by reaction of 50 g. (0.32 mole) commercial 2,5-dimercapto-1,3,4-thiadiazole with 26.4 g (0.66 mole) sodium hydroxide in 400 ml refluxing isopropanol followed by the addition of 110 g (0.66 mole) 1-bromohexane. After removal of the solid precipitate (sodium bromide), 71.7 g of product was isolated by vacuum stripping. The product was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04216100
Source datasetuspto-grants-1980_08
ORD IDord-8bcb92134641468c81750f369109f0ee
Source noteuspto-grants-1980_08