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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903401Generated: November 2, 2026

Epichlorohydrin → HCID 13064030, compound

https://huagongshe.com/reaction/1903401

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEpichlorohydrinHCID 7835—
ReactantSodium HydroxideHCID 14798—
Reactant2,1,3-Benzothiadiazol-4-olHCID 4914673—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 13064030HCID 1306403069%

Reaction Steps

7.6 g (50 mM) 4-hydroxy-2,1,3-benzthiadiazole were dissolved in 100 ml. dioxan and mixed with 50 ml. epichlorohydrin and 55 ml. 1 N aqueous sodium hydroxide solution and the reaction mixture stirred for 4-5 hours at 55°-60° C. When the reaction was finished, the reaction mixture was diluted with 300 ml. water and extracted with chloroform. The dried chloroform solution was evaporated and the residue was chromatographed on a silica gel column (elution agent: chloroform). The residue obtained after evaporation of the elution fractions crystallized upon treatment with diisopropyl ether. There were obtained 7.2 g (69% of theory) 4-(2,3-epoxypropyloxy)-2,1,3-benzthiadiazole, which had a melting point of 65°-67° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436742
Source datasetuspto-grants-1984_03
ORD IDord-4a7e93af69464f2bbc582b39b810da39
Source noteuspto-grants-1984_03