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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Selenium Dioxide | HCID 24007 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | N-(3-acetylphenyl)benzenesulfonamide | HCID 738634 | — |
| Product | N-[3-(2-ethoxy-2-hydroxyacetyl)-phenyl]-benzenesulphonamide | HCID 57429080 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07754756B2 |
|---|
| Source dataset | uspto-grants-2010_07 |
|---|
| ORD ID | ord-72f9a18a817b4c1c844f32f6b41f310f |
|---|
| Source note | uspto-grants-2010_07 |
|---|