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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1890524Generated: November 2, 2026

Methyl 5-methyl-4-nitrothiophene-2-carboxylate → Methyl 4-amino-5-methylthiophene-2-carboxylate

https://huagongshe.com/reaction/1890524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-methyl-4-nitrothiophene-2-carboxylateHCID 268679—
CatalystNickelHCID 935—
SolventMeOH tetrahydrofuranHCID 21899815—
ProductMethyl 4-amino-5-methylthiophene-2-carboxylateHCID 5964074764.3%

Reaction Steps

To a solution of methyl 5-methyl-4-nitrothiophene-2-carboxylate (F-3) (14.8 g, 73.6 mmol) in MeOH/THF (1:1, 300 mL) was added Raney Ni. The reaction mixture was degassed and charged with hydrogen 3 times, and then stirred at room temperature for 36 h under 1 atmosphere of hydrogen. Raney Ni was filtered, and the filtrate was concentrated. The residue was treated with aqueous HCl (1 N, 150 mL) and filtered. The filtrate was treated with aqueous NaOH (1 N) to bring pH to about 8 to 9. Then the mixture was extracted with ethyl acetate. The combined organic layers were dried over Na2SO4, and the solvent was removed to give the title compound (8.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08507487B2
Source datasetuspto-grants-2013_08
ORD IDord-9ee0c8f6491d4a399659f1d71df5922e
Source noteuspto-grants-2013_08