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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202664Generated: October 31, 2026

Carbon Dioxide → 4-Methylthiophene-3-carboxylic acid

https://huagongshe.com/reaction/2202664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant3-Bromo-4-methylthiopheneHCID 2734935—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product4-Methylthiophene-3-carboxylic acidHCID 12993673—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of 3-bromo-4-methylthiophene (2.7 g, 15.6 mmol) in THF (35 mL) was added n-BuLi (1.6 M in hexane, 14.6 mL, 23.3 mmol) at −78° C. dropwise over a period of 15 min and the mixture was stirred at −78° C. for 30 min. The CO2 (gaseous) was passed through the reaction mixture for 10 min and the mixture was stirred at the same temperature for 20 min. Thereafter, the reaction mixture was warmed to 0° C., quenched with aqueous 1 M NaOH (60 mL) and washed with EtOAc (2×50 mL). The aqueous layer was acidified to pH ˜5 and extracted with DCM (2×50 mL). The combined organic layers were washed with water (100 mL), brine (100 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by column chromatography (silica gel, 8% MeOH/DCM as eluent) to provide compound A56-1 (1.5 g, 70%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365522B2
Source datasetuspto-grants-2016_06
ORD IDord-bbffdb27d6504c7ead4ae168e3d3f1b1
Source noteuspto-grants-2016_06