HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753676Generated: October 27, 2026
Hydrogen Peroxide → Bis(4-butoxyphenyl) sulfoxide
https://huagongshe.com/reaction/1753676
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Thiosulfate Pentahydrate | HCID 61475 | — |
| Reactant | Bis(4-butoxyphenyl) sulfide | HCID 117666789 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | Bis(4-butoxyphenyl) sulfoxide | HCID 20458150 | 90% |
Reaction Steps
In 200 g of acetic acid was dissolved 30 g of bis(4-butoxyphenyl) sulfide obtained in Synthesis Example 1-17. While the solution was maintained at an internal temperature of 30° C., 8.8 g of 35 wt % aqueous hydrogen peroxide was added dropwise. The reaction solution was aged at room temperature for 12 hours, after which under ice cooling, a mixture of 0.9 g sodium thiosulfate pentahydrate and 30 g water was added dropwise to quench the reaction. The solution was combined with 200 g of methylene chloride and 50 g of water for extraction. The organic layer was separated, washed with water, and concentrated in vacuum. On subsequent purification by silica gel chromatography, 28 g of the target compound, bis(4-butoxyphenyl) sulfoxide was obtained as amorphous solid. Yield 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09164384B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-a98881cdb0b34a8c97a415ee9a73d5d8 |
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| Source note | uspto-grants-2015_10 |
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