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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845516Generated: October 30, 2026

Sodium Thiosulfate → HCID 178493773, compound

https://huagongshe.com/reaction/845516

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 178493767HCID 178493767—
SolventSodium HydroxideHCID 14798—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178493773HCID 178493773—

Reaction Steps

0.8 g of 2-[(4,5-dimethoxy-2-pyridyl)methylthio]-5-(2,2,2-trifluoroethoxy)-1H-benzimidazole is dissolved in 15 ml of dioxane and 2.5 ml of 1N sodium hydroxide solution. A mixture of 3 ml of 8% strength sodium hypochlorite solution and 3.5 ml of 1N sodium hydroxide solution are added dropwise in the course of 2 hours, while cooling to 0°-5° C. After addition of 5 ml of 5% strength sodium thiosulfate solution, the mixture is concentrated to dryness, the residue is taken up in water and the mixture is brought to pH 7 with phosphate buffer. The solid which has precipitated out is filtered off with suction, dried and recrystallized from ethyl acetate/diisopropyl ether. 0.45 g (55% of theory) of the title compound is obtained as colorless crystals of m.p. 142°-143° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04758579
Source datasetuspto-grants-1988_07
ORD IDord-e6b3026bfe074d7c8efc35c53af78772
Source noteuspto-grants-1988_07