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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1583998Generated: November 4, 2026

Sodium Hydroxide → HCID 178493216, compound

https://huagongshe.com/reaction/1583998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium ThiosulfateHCID 24477—
ReactantAmmonium SulfateHCID 6097028—
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 178493202HCID 178493202—
SolventEthyl AcetateHCID 8857—
ProductHCID 178493216HCID 17849321685%

Reaction Steps

A mixture of 8.5 ml of commercially available sodium hypochlorite solution (about 15% of active chlorine) and 6 ml of 10% strength sodium hydroxide solution is added dropwise to a solution of 1.5 g 2-[(4-methoxy-2-pyridyl)methylthio]-5-(1,1,2,2-tetrafluoroethoxy)-1H-benzimidazole in 30 ml of ethyl acetate at 0° C. in the course of 20 min., stirring is continued at this temperature for 20 min. and 0.6 ml of 10% strength sodium thiosulfate solution is then added. 1.5 g of ammonium sulfate are added and the organic phase is separated off, washed with saturated sodium chloride solution, dried with magnesium sulfate and concentrated to a small volume. 1.3 g (85%) of the title compound of melting point 131°-132° C. (decomposition) are obtained by precipitation with diisopropyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04555518
Source datasetuspto-grants-1985_11
ORD IDord-b7f778150f854f568c2c70dd1fdb0e85
Source noteuspto-grants-1985_11