Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357741Generated: October 29, 2026

Water → 5-Methanesulfonylthiophene-2-carboxylic acid

https://huagongshe.com/reaction/357741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantSodium SulfiteHCID 24437—
Reactant5-(Methylsulfanyl)thiophene-2-carbaldehydeHCID 2736997—
ReactantSodium ChloriteHCID 23668197—
ReactantMonosodium phosphateHCID 23672064—
SolventHydrogen PeroxideHCID 784—
SolventAcetonitrileHCID 6342—
Product5-Methanesulfonylthiophene-2-carboxylic acidHCID 2740497—

Reaction Steps

5-Methylthio-2-thiophenecarbaldehyde (4.48 g) (synthesized in accordance with the method described in Tetrahydron, 41, 3803 (1985)) was dissolved in acetonitrile (20 ml), and sodium dihydrogen phosphate (1.2 g) in water (10 ml) and 30% aqueous hydrogen peroxide (3.5 ml) were added. Further sodium chlorite (3.85 g) in water (10 ml) was added dropwise under ice-cooling. The mixture was stirred at room temperature for 15 hours, and sodium sulfite (1 g) was added. The mixture was alkalified with 1N aqueous sodium hydroxide and extracted with diethyl ether. The aqueous layer was acidified with 1N hydrochloric acid and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was recrystallized from ethyl acetate-diisopropyl ether to give 5-methanesulfonyl-2-thiphenecarboxylic acid (1.73 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840917
Source datasetuspto-grants-1998_11
ORD IDord-b1df5942a1d24aaea02ea1320bbdd56c
Source noteuspto-grants-1998_11