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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 607435Generated: October 30, 2026

Methanol → Methyl 3-(methylsulfinyl)benzeneacetate

https://huagongshe.com/reaction/607435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
Reactant[3-(Methanesulfinyl)phenyl]acetic acidHCID 45925729—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 3-(methylsulfinyl)benzeneacetateHCID 5765798182%

Reaction Steps

A solution of [3-(methylsulfinyl)phenyl]acetic acid (1.31 g, 6.60 mmol) and carbonyldiimidazole (1.18 g, 7.26 mmol) in 25.0 mL THF was stirred at room temperature for 15 minutes, then methanol (2.1 mL, 52.8 mmol) was added. After 10 minutes the reaction was briefly warmed to near reflux temperature, then allowed to cool to room temperature. After 20 minutes, the reaction was partitioned between EtOAc and NaHCO3/brine mixture. The EtOAc layer was washed with dilute brine, dilute HCl solution, brine, dried with anhydrous Na2SO4 and rotary evaporated to give the title compound as a yellow-orange oil (1.14 g, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07915443B2
Source datasetuspto-grants-2011_03
ORD IDord-e2cce02325f6490991ce63502e08cb13
Source noteuspto-grants-2011_03