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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450031Generated: October 25, 2026

Methyl 5-nitrothiophene-3-carboxylate → Methyl 5-aminothiophene-3-carboxylate

https://huagongshe.com/reaction/450031

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 5-nitrothiophene-3-carboxylateHCID 2740231—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
ProductMethyl 5-aminothiophene-3-carboxylateHCID 1898362624%

Reaction Steps

To a solution of 5-nitro-thiophene-3-carboxylic acid methyl ester (0.5 g, 2.67 mmol) in aqueous acetic acid (5 ml) was added iron powder (1.04 g, 18.6 mmol) and the reaction mixture was heated to reflux for 3 hr. The reaction mixture was filtered and triethylamine was added to the filtrate. The compound was extracted with ethyl acetate and the organic layer was washed with water, concentrated and dried to yield crude compound. The compound was purified by silica gel column chromatography, using ethyl acetate/hexane as eluent, to yield 5-amino-thiophene-3-carboxylic acid methyl ester (0.1 g, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08486962B2
Source datasetuspto-grants-2013_07
ORD IDord-8665354c5f57499a8919b68a4dabffcf
Source noteuspto-grants-2013_07