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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418248Generated: November 2, 2026

Sodium Hypochlorite → HCID 178493208, compound

https://huagongshe.com/reaction/2418248

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HypochloriteHCID 23665760—
ReactantHCID 178493199HCID 178493199—
SolventEthyl AcetateHCID 8857—
ProductHCID 178493208HCID 178493208—

Reaction Steps

600 ml of a 1.5% strength aqueous sodium hypochlorite solution are added within 3 minutes at 10° C. with vigorous stirring to a solution of 16.2 g (0.048 mole) of 5-trifluoromethyl-2-[(4-methoxy-2-pyridylmethyl)thio]-(1H)-benzimidazole in 960 ml of ethyl acetate. The mixture is then stirred for a further 2 minutes. The organic phase is separated off and is washed with 100 ml of distilled water. The aqueous phase is adjusted to pH 7-8 by addition of glacial acetic acid and is then extracted three times with ethyl acetate. The extracts are washed with water and the combined organic phases are then concentrated to a volume of 100 ml and cooled in an ice bath. The precipitate which has separated out is filtered off with suction and washed with cold ethyl acetate. Yield: 13.2 g of m.p. 166° C. (decomposition).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04472409
Source datasetuspto-grants-1984_09
ORD IDord-3161bf00f1c445f09e9f2e4a1df63353
Source noteuspto-grants-1984_09