Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 357768Generated: October 25, 2026

Dimethylformamide → 2,5-Dimethylthiophene-3-carbaldehyde

https://huagongshe.com/reaction/357768

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2,5-DimethylthiopheneHCID 12514—
ReactantPhosphorus oxychlorideHCID 24813—
SolventWaterHCID 962—
Product2,5-Dimethylthiophene-3-carbaldehydeHCID 276275910.1%

Reaction Conditions

Temperature100 °C

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-5f2562df807c47ee9af68f2b2cff287a
Source noteuspto-grants-1998_11