HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719911Generated: October 30, 2026
Hydrogen Peroxide → 2-(3-Chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid
https://huagongshe.com/reaction/719911
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | 2-(3-Chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-propionic acid | HCID 12067653 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | 2-(3-Chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid | HCID 12067654 | 99.1% |
Reaction Steps
A mixture of 2-(3-chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-propionic acid (4.14 g, 13.85 mmol) in formic acid (7.08 mL) was cooled to 0° C. and then treated with a 30% aqueous hydrogen peroxide solution (7.85 μL). Tetrahydrofuran (4 mL) was added to help solubilize the starting material. The resulting reaction mixture was allowed to warm to 25° C. where it was stirred overnight. The reaction mixture was then cooled to 0° C. and slowly treated with a saturated aqueous sodium sulfite solution. The product was extracted into ethyl acetate (3×20 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo to afford 2-(3-chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid (4.54 g, 99.1%) as a white solid: mp 123.9–126.2° C.; FAB-HRMS m/e calcd for C15H19ClO4S (M+H)+ 331.0771, found 331.0776.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07132425B2 |
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| Source dataset | uspto-grants-2006_11 |
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| ORD ID | ord-11e74ab2c2914337b6f136abb8df99e9 |
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| Source note | uspto-grants-2006_11 |
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