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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632485Generated: November 3, 2026

Allyl bromide → HCID 20443108, compound

https://huagongshe.com/reaction/1632485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodiumHCID 5360545—
Reactant(5-Chloro-2,1,3-benzothiadiazol-4-yl)cyanamideHCID 13785516—
SolventEthanolHCID 702—
ProductHCID 20443108HCID 20443108—

Reaction Steps

The starting material is obtained as follows: 5 g 5-chloro-N-cyano-2,1,3-benzothiadiazol-4-amine are added to a solution of 0.55 g sodium in 60 ml ethanol and the mixture is reacted with 3 g allyl bromide. The mixture is agitated 3 hours under refluxing and the solvent evaporated under vacuum. The residue is extracted with methylene chloride. N-allyl-5-chloro-N-cyano-2,1,3-benzothiadiazol-4-amine (M.P. 62°-63°) is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04476135
Source datasetuspto-grants-1984_10
ORD IDord-a93c9c0d514d4bd39fa8e8327b010cca
Source noteuspto-grants-1984_10