HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256388Generated: October 29, 2026
Hydrogen Peroxide → 5-{2-[2-(2-Methoxyphenoxy)-ethylamino]-1-phenylsulfinylethyl}-2-methylbenzenesulfonamide
https://huagongshe.com/reaction/256388
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | HCID 13118104 | HCID 13118104 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-{2-[2-(2-Methoxyphenoxy)-ethylamino]-1-phenylsulfinylethyl}-2-methylbenzenesulfonamide | HCID 13106272 | — |
Reaction Steps
In 20 ml of acetic acid was dissolved 2 g of 5-{2-[2-(2-methoxyphenoxy)ethylamino]-1-phenylthioethyl}-2-methylbenzenesulfonamide and after adding thereto 0.5 ml of 30% H2O2, the mixture was heated to 50°-60° C. for 3 hours. After adding thereto 100 ml of water, the reaction mixture was extracted with 200 ml of ethyl acetate. The ethyl acetate extract was washed with an aqueous 1% sodium carbonate solution and then ethyl acetate was distilled off under reduced pressure. The residue was applied to a silica gel column chromatography, the product was eluted with a mixed solvent of chloroform and methanol (9:1 by volume ratio), and the colorless viscous oily product thus obtained was crystallized by the addition of ethyl acetate. The crystals formed were recovered by filtration to provide 1.3 g of 5-{2-[2-(2-methoxyphenoxy)ethylamino]-1-phenylsulfinylethyl}-2-methylbenzenesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04703063 |
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| Source dataset | uspto-grants-1987_10 |
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| ORD ID | ord-1bf573c5e8854e079664a159226f5989 |
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| Source note | uspto-grants-1987_10 |
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