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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1843013Generated: October 31, 2026

Formic Acid → Methyl 2-(3-chloro-4-(methylsulfonyl)phenyl)propanoate

https://huagongshe.com/reaction/1843013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormic AcidHCID 284—
ReactantHydrogen PeroxideHCID 784—
ReactantWaterHCID 962—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantMethyl 2-(3-chloro-4-(methylthio)phenyl)propanoateHCID 70816255—
ProductMethyl 2-(3-chloro-4-(methylsulfonyl)phenyl)propanoateHCID 70816425—

Reaction Conditions

Temperature0 °C

Reaction Steps

Formic acid (20.8 mL, 1 eq) was added to methyl 2-(3-chloro-4-(methylthio)phenyl)propanoate (3.2 g, crude) and cooled to 0° C. Hydrogen peroxide (4.48 mL, 3 eq) was added drop wise at 0° C. and the reaction mass was stirred for overnight at room temperature. Progress of the reaction was monitored by TLC (30% ethyl acetate/hexane, Rf˜0.3). On completion of the reaction, the contents were cooled to 0° C., water was added and the mixture was extracted with ethyl acetate (2×100 mL). The combined extract was washed with NaHCO3 solution, dried over sodium sulfate and concentrated under reduced pressure to obtain methyl 2-(3-chloro-4-(methylsulfonyl)phenyl)propanoate as a colorless thick liquid (3.2 g, crude). Crude product obtained was directly used for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946204B2
Source datasetuspto-grants-2015_02
ORD IDord-5652495a18a94bc29362de670cb781be
Source noteuspto-grants-2015_02