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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2377251Generated: November 2, 2026

Methanol → 4-Bromo-2-thiophenecarboxylic Acid

https://huagongshe.com/reaction/2377251

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSulfuric AcidHCID 1118—
Reactant4-Bromothiophene-2-carbaldehydeHCID 87792—
Catalystchromium (VI) trioxideHCID 10219390—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product4-Bromo-2-thiophenecarboxylic AcidHCID 610409—

Reaction Conditions

Temperature5 °C

Reaction Steps

To a solution of chromium(VI)oxide (1.57 g, 15.70 mmol) in water (3 mL) was added dropwise concentrated sulfuric acid (1.3 mL, 23.55 mmol). The formed precipitate was re-dissolved by slow addition of the minimum required amount of water and the solution was cooled with an ice bath. This solution was then added dropwise to a solution of 4-bromo-2-thiophenecarboxaldehyde (2.0 g, 10.47 mmol) in acetone (20 mL) at about 5° C. The reaction mixture was stirred at about 5° C. for about 30 minutes and then at room temperature for about 2 hours. Methanol (30 mL) was added to the reaction mixture to destroy excess oxidant and the formed solids were collected by filtration. The filtrate was concentrated under vacuum and the residue was partitioned between diethyl ether and water. The organic extract was washed with water and brine, dried (MgSO4), filtered and concentrated under vacuum to provide the desired product. MS (DCI-NH3): m/z 206, 208 (M)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468371B2
Source datasetuspto-grants-2008_12
ORD IDord-8a5f1571307e46ca82ed734996cd57a5
Source noteuspto-grants-2008_12