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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300923Generated: October 27, 2026

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

https://huagongshe.com/reaction/2300923

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 numberUS06498185B1
Source datasetuspto-grants-2002_12
ORD IDord-6c8ce71a0b4649948576ed73acd34f92
Source noteuspto-grants-2002_12