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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281790Generated: October 27, 2026

Hydrochloric Acid → Ethyl 2-(6-amino-2,3-dichloroanilino)benzo[b]thiophene-3-carboxylate

https://huagongshe.com/reaction/1281790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant2,3,4-TrichloronitrobenzeneHCID 28697—
ReactantStannous chloride dihydrateHCID 61436—
ReactantEthyl 2-amino-1-benzothiophene-3-carboxylateHCID 699464—
ReactantEthyl 2-(2,3-dichloro-6-nitroanilino)benzo[b]thiophene-3-carboxylateHCID 18422195—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
ProductEthyl 2-(6-amino-2,3-dichloroanilino)benzo[b]thiophene-3-carboxylateHCID 18422327—

Reaction Steps

In the same manner as in Starting Material Synthesis Example 4 and using ethyl 2-aminobenzo[b]thiophene-3-carboxylate (6.6 g), 2,3,4-trichloronitrobenzene (7.0 g) and dimethyl sulfoxide (70 ml), crude crystals (12 g) of ethyl 2-(2,3-dichloro-6-nitroanilino)benzo[b]thiophene-3-carboxylate were obtained. Without purification, in the same manner as in Starting Material Synthesis Example 21 and using ethanol (40 ml), 18% hydrochloric acid (60 ml) and tin(II) chloride-dihydrate (24.6 g), ethyl 2-(6-amino-2,3-dichloroanilino)benzo[b]thiophene-3-carboxylate (4.2 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455521B1
Source datasetuspto-grants-2002_09
ORD IDord-fdfa5a0ff45b4bd6b0fc9d2d08374388
Source noteuspto-grants-2002_09