HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 845516Generated: October 30, 2026
Sodium Thiosulfate → HCID 178493773, compound
https://huagongshe.com/reaction/845516
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | HCID 178493767 | HCID 178493767 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178493773 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04758579 |
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| Source dataset | uspto-grants-1988_07 |
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| ORD ID | ord-e6b3026bfe074d7c8efc35c53af78772 |
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| Source note | uspto-grants-1988_07 |
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