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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357769Generated: October 27, 2026

Sodium Hydroxide → 2,5-Dimethylthiophene-3-carboxylic acid

https://huagongshe.com/reaction/357769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,5-Dimethylthiophene-3-carbaldehydeHCID 2762759—
ReactantMonosodium phosphateHCID 23672064—
SolventHydrogen PeroxideHCID 784—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2,5-Dimethylthiophene-3-carboxylic acidHCID 819559261.8%

Reaction Steps

Phosphorus oxychloride (10 ml) was slowly added dropwise to dimethylformamide (30 g) under ice-cooling, and 2,5-dimethylthiophene (11.2 g) was added. The mixture was stirred at 100° C. for 15 hours, poured into water and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 2,5-dimethyl-3-thiophenecarbaldehyde (1.41 g). 2,5-Dimethyl-3-thiophenecarbaldehyde (3.89 g) synthesized in this manner was dissolved in acetonitrile (30 ml), and sodium dihydrogen phosphate (1.2 g) in water (15 ml) and 30% aqueous hydrogen peroxide (3.5 ml) were added dropwise. The mixture was stirred at room temperature for 2 hours, alkalified with 1N aqueous sodium hydroxide and washed 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 to give 2,5-dimethyl-3-thiophenecarboxylic acid (4.09 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840917
Source datasetuspto-grants-1998_11
ORD IDord-9f534f451f654a38b945d089223ed77d
Source noteuspto-grants-1998_11