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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 253195Generated: October 25, 2026

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

https://huagongshe.com/reaction/253195

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. A total of 18.37 g of 5-amino-benzo[b]thiophene-2-carboxylic acid ethyl ester was obtained. MS (EI): cal'd 222.0 (MH+), exp 222.2 (MH+). Procedure for Acylation

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07872024B2
Source datasetuspto-grants-2011_01
ORD IDord-305413ff6bf14c38a2a1d4db9d30a2bf
Source noteuspto-grants-2011_01