HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753682Generated: October 28, 2026
Hydrogen Peroxide → HCID 117666755, compound
https://huagongshe.com/reaction/1753682
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Thiosulfate Pentahydrate | HCID 61475 | — |
| Reactant | HCID 117666794 | HCID 117666794 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 117666755 | HCID 117666755 | 86% |
Reaction Steps
In 85 g of acetic acid was dissolved 12 g of 4-(2-methoxyethoxy)phenyl phenyl sulfide obtained in Synthesis Example 1-29. While the solution was maintained at an internal temperature of 30° C., 4.5 g of 35 wt % aqueous hydrogen peroxide was added dropwise. The reaction solution was aged at room temperature for 18 hours, after which under ice cooling, a mixture of 1.2 g sodium thiosulfate pentahydrate and 15 g water was added dropwise to quench the reaction. The solution was combined with 80 g of methylene chloride and 40 g of water for extraction. The organic layer was separated, washed with water, and concentrated in vacuum. On subsequent crystallization from ethyl acetate/hexane, 11 g of the target compound, 4-(2-methoxyethoxy)phenyl phenyl sulfoxide was obtained as white crystals. Yield 86%.
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-e01733a25fa84cc68fdbea5bfac20a54 |
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| Source note | uspto-grants-2015_10 |
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