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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844163Generated: October 27, 2026

Nitric Acid → 2-Carboxy-3-methyl-5-nitrothiophene

https://huagongshe.com/reaction/844163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitric AcidHCID 944—
Reactant3-Methyl-2-thenoic acidHCID 90269—
ReactantSodium BicarbonateHCID 516892—
SolventTrifluoroacetic acidHCID 6422—
Product2-Carboxy-3-methyl-5-nitrothiopheneHCID 1837695753%

Reaction Steps

To a solution of 2-carboxy-3-methylthiophene (10 g, 70.3 mmol) in 80 mL of trifluoroacetic acid at 0° C. was added HNO3 (1.2 mL,1.0 eq.) dropwise. The reaction mixture was warmed to ambient temperature and after 4 hours another 1.0 eq. of HNO3 was added. The reaction mixture was made basic with aqueous sodium bicarbonate and washed with ethyl acetate. The aqueous layer was acidified with concentrated HCl and extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated in vacuo to afford 5.75 g (53%) of 2-carboxy-3-methyl-5-nitrothiophene and 2-carboxy-3-methyl-4-nitrothiophene, as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380221B1
Source datasetuspto-grants-2002_04
ORD IDord-dc737adc7dc448e598b6371f8d8d050a
Source noteuspto-grants-2002_04