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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099669Generated: October 25, 2026

Methanol → Methyl 3-(4-(methylsulfinyl)phenyl)propanoate

https://huagongshe.com/reaction/1099669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethyl 3-(4-(methylthio)phenyl)propanoateHCID 21914741—
ProductMethyl 3-(4-(methylsulfinyl)phenyl)propanoateHCID 5765789781%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a 250 mL round bottom flask, methyl 3-(4-(methylthio)phenyl)propanoate (0.50 g, 2.38 mmol) was dissolved in MeOH under a N2(g). The resulting solution was cooled to 0° C., then 0.5 M NaIO4 (4.76 mL, 2.38 mmol) was added dropwise to the cooled solution causing the formation of a white precipitate. The reaction was allowed to warm to room temperature. When HPLC indicated complete consumption of starting thioether, the reaction was filtered and the filtrate was concentrated. The resulting residue was taken up in CHCl3 (25 mL) then extracted with brine. The brine layer was subsequently extracted with CHCl3 (2×25 mL). The combined organic extracts were then dried over anhydrous Na2SO4(s), filtered and concentrated. The resulting sulfoxide was then purified by passing through a plug of silica using EtOAc/Hexanes as eluant affording methyl 3-(4-(methylsulfinyl)phenyl)propanoate (0.436 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143410B2
Source datasetuspto-grants-2012_03
ORD IDord-dcb3ba5dafb74dc7bb34b5432ccc9fe6
Source noteuspto-grants-2012_03