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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281788Generated: October 27, 2026

Hydrochloric Acid → Ethyl 2-(2-amino4,5-dichloroanilino)benzo[b]thiophene-3-carboxylate

https://huagongshe.com/reaction/1281788

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,4,5-TrichloronitrobenzeneHCID 6983—
ReactantStannous chloride dihydrateHCID 61436—
ReactantEthyl 2-amino-1-benzothiophene-3-carboxylateHCID 699464—
ReactantEthyl 2-(4,5-dichloro-2-nitroanilino)benzo[b]thiophene-3-carboxylateHCID 18422321—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
ProductEthyl 2-(2-amino4,5-dichloroanilino)benzo[b]thiophene-3-carboxylateHCID 18422259—

Reaction Steps

In the same manner as in Starting Material Synthesis Example 4 and using ethyl 2-aminobenzo[b]thiophene-3-carboxylate (6.0 g), 2,4,5-trichloronitrobenzene (6.8 g) and dimethyl sulfoxide (70 ml), crude crystals (10.3 g) of ethyl 2-(4,5-dichloro-2-nitroanilino)benzo[b]thiophene-3-carboxylate were obtained. Without purification, in the same manner as in Starting Material Synthesis Example 21 and using ethanol (100 ml), 18%hydrochloric acid (100 ml) and tin(II) chloride-dihydrate (22.8 g), ethyl 2-(2-amino-4,5-dichloroanilino)benzo[b]thiophene-3-carboxylate (5.3 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455521B1
Source datasetuspto-grants-2002_09
ORD IDord-ded1db50a42441b69d876a3bf4465b91
Source noteuspto-grants-2002_09