Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876777Generated: October 30, 2026

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

https://huagongshe.com/reaction/876777

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 numberUS08987269B2
Source datasetuspto-grants-2015_03
ORD IDord-205a3e312cf948db8d02c967d690a325
Source noteuspto-grants-2015_03