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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986650Generated: November 3, 2026

Methyl 7-nitrobenzo[b]thiophene-2-carboxylate → Methyl 7-amino-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/1986650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 7-nitrobenzo[b]thiophene-2-carboxylateHCID 57722418—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
ProductMethyl 7-amino-1-benzothiophene-2-carboxylateHCID 45089769100%

Reaction Steps

7-Nitro-benzo[b]thiophene-2-carboxylic acid methyl ester (1 g, 4.22 mmol) was suspended in EtOAc (40 mL) and a suspension of 10% Pd/C (400 mg) in 20 mL EtOAc was added. Hydrogen gas was introduced into the flask from an H2-filled balloon attached to a needle inserted through a septum. The black suspension was stirred 12 h at room temperature. After stirring 12 h, the black suspension was filtered through diatomaceous earth and the filter cake was washed several times with EtOAc. The combined filtrates were dried (MgSO4), filtered and the solvent was removed to afford 7-amino-benzo[b]thiophene-2-carboxylic acid methyl ester as a yellow solid (860 mg, 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550461B2
Source datasetuspto-grants-2009_06
ORD IDord-902c04a3c0be420d8688b6029100b3d9
Source noteuspto-grants-2009_06