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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2355238Generated: October 26, 2026

Methane → N-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamide

https://huagongshe.com/reaction/2355238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantWaterHCID 962—
ReactantSelenium DioxideHCID 24007—
Reactant1,4-DioxaneHCID 31275—
ReactantN-(3-acetylphenyl)benzenesulfonamideHCID 738634—
ProductN-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamideHCID 57429080—

Reaction Conditions

Temperature80 °C

Reaction Steps

1 ml of water, 1 g activated charcoal and 2.66 g (24 mmol) selenium dioxide are added to a solution of 1.65 g (6 mmol) N-(3-acetyl-phenyl)-benzenesulphonamide in 10 ml dioxane. The reaction mixture is stirred for 4 days at 80° C. and then concentrated by evaporation in the rotary evaporator. The residue is dissolved in 30 ml of ethanol and refluxed for 4 hours. Then the reaction mixture is concentrated by evaporation in the rotary evaporator. The residue is dissolved in 100 ml of ethyl acetate, washed several times with 30 ml saturated, aqueous sodium hydrogen carbonate solution, dried on sodium sulphate and again concentrated by evaporation in the rotary evaporator. The crude product thus obtained as a yellow solid is reacted further without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07754756B2
Source datasetuspto-grants-2010_07
ORD IDord-72f9a18a817b4c1c844f32f6b41f310f
Source noteuspto-grants-2010_07