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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172866Generated: November 2, 2026

Ethyl 5-nitro-1-benzothiophene-2-carboxylate → Ethyl 5-amino-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/1172866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-nitro-1-benzothiophene-2-carboxylateHCID 737499—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl 5-amino-1-benzothiophene-2-carboxylateHCID 2764450—

Reaction Steps

A suspension of 5-nitro-benzo[b]thiophene-2-carboxylic acid ethyl ester (10.52 g, 41.89 mmol) and 10% Pd/C (1.1 g) in 450 mL of EtOH was hydrogenated under 1 atm of H2 for 4 d at rt. The reaction mixture was filtered and the filtrate was concentrated and dried to give 5-amino-benzo[b]thiophene-2-carboxylic acid ethyl ester as a green solid. A parallel reaction was preformed on 10.61 g of 5-nitro-benzo[b]thiophene-2-carboxylic acid ethyl ester in the same manner. 5-amino-benzo[b]thiophene-2-carboxylic acid ethyl ester was obtained. MS (EI): cal'd 222.0 (MH+), exp 222.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834034B2
Source datasetuspto-grants-2010_11
ORD IDord-fa8b0c1a61594e479ff9c81e18f83cb4
Source noteuspto-grants-2010_11