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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium SulfiteHCID 24437—
Reactant2-(3-Chloro-4-methylsulfanyl-phenyl)-3-cyclopentyl-propionic acidHCID 12067653—
SolventFormic AcidHCID 284—
Product2-(3-Chloro-4-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acidHCID 1206765499.1%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132425B2
Source datasetuspto-grants-2006_11
ORD IDord-11e74ab2c2914337b6f136abb8df99e9
Source noteuspto-grants-2006_11