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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512110Generated: October 29, 2026

Dichloromethane → HCID 44219554, compound

https://huagongshe.com/reaction/512110

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantSodium PyrosulfiteHCID 656671—
ReactantHCID 44219243HCID 44219243—
ProductHCID 44219554HCID 4421955487%

Reaction Steps

4.6 g (12.7 mM) of 5-bromo-3-[(4-chlorobenzyl)thio]-1-ethylpyrazin-2(1H)-one and 9.9 g (40 mM) of metachloroperbenzoic acid (70%) in 75 ml of dichloromethane were stirred for 10 min at room temperature. Aqueous 2M solution of sodium metabisulphite was added, the organic layer was separated and washed with an aqueous solution of hydrogenocarbonate, then with water and evaporated under vacuum. The residue was taken up in diisopropyle oxide. A solid was filtered and washed with diisopropyle oxide, to give 4.3 g of 5-bromo-3-[(4-chlorobenzyl)sulfonyl]-1-ethylpyrazin-2(1H)-one. Yield: 87%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102632B2
Source datasetuspto-grants-2015_08
ORD IDord-f26e3e71e412452fb3a2321f2f825880
Source noteuspto-grants-2015_08