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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846682Generated: October 30, 2026

Ethanol → HCID 19764854, compound

https://huagongshe.com/reaction/846682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantPotassium peroxymonosulphateHCID 10313463—
ReactantHCID 19764842HCID 19764842—
ProductHCID 19764854HCID 1976485482%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of potassium peroxymonosulphate (17.7 g) in water (30 ml) was added to a mixture of 3-bromophenyl 2-naphthyl sulphide (3 g) and ethanol (30 ml) which had been cooled to 0° C. in an ice-bath. The mixture was stirred at ambient temperature for 18 hours and at 60° C. for 5 hours. The mixture was cooled to ambient temperature and partitioned between chloroform and water. The organic phase was dried (MgSO4) and evaporated to give 3-bromophenyl 2-naphthyl sulphone (2.7 g, 82%) as a solid which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137913
Source datasetuspto-grants-1992_08
ORD IDord-6d64755f2000405a8e103af310aea8e7
Source noteuspto-grants-1992_08