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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986647Generated: October 27, 2026

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

https://huagongshe.com/reaction/1986647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 7-nitrobenzo[b]thiophene-2-carboxylateHCID 57722418—
SolventAcetic AcidHCID 176—
SolventHydrochloric AcidHCID 313—
ProductMethyl 7-amino-1-benzothiophene-2-carboxylateHCID 45089769100%

Reaction Steps

To a mixture of 7-nitro-benzo[b]thiophene-2-carboxylic acid methyl ester (100 mg) in acetic acid (4 mL) was added a solution of SnC2.2H2O (10 eq) in 1.5 mL of concentrated HCl. The reaction was stirred at room temperature 12 h. The excess acid was partially removed in vacuo, and the reaction mixture was then poured into a flask (250 mL) and was neutralized with saturated NaHCO3 solution at 0° C. The pH was brought up to pH 9 by adding solid NaHCO3. The resulting aqueous mixture was diluted with EtOAc, and the Tin-by product was removed by filtering through a pad of diatomaceous earth. The pad was rinsed with EtOAc and the combined filtrates were partitioned in a separatory funnel. The aqueous layer was extracted with EtOAc two times times. The combined organics were dried over MgSO4, filtered and concentrated to give the desired 7-amino-benzo[b]thiophene-2-carboxylic acid methyl ester (100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07550461B2
Source datasetuspto-grants-2009_06
ORD IDord-3be63abe472f44f9b1eb7d94f1922fc9
Source noteuspto-grants-2009_06