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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649924Generated: October 25, 2026

Hydrochloric Acid → Ethyl 2-(2-aminoanilino)-6-methylbenzo[b]thiophene-3-carboxylate

https://huagongshe.com/reaction/649924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantStannous cationHCID 104883—
ReactantEthyl 2-amino-6-methylbenzo[b]thiophene-3-carboxylateHCID 18422153—
ReactantEthyl 6-methyl-2-(2-nitroanilino)benzo[b]thiophene-3-carboxylateHCID 18422322—
SolventDimethyl SulfoxideHCID 679—
SolventEthanolHCID 702—
ProductEthyl 2-(2-aminoanilino)-6-methylbenzo[b]thiophene-3-carboxylateHCID 18422261—

Reaction Steps

In the same manner as in Starting Material Synthesis Example 4 and using ethyl 2-amino-6-methylbenzo[b]thiophene-3-carboxylate (4.18 g), 2-fluoronitrobenzene (2.5 g) and dimethyl sulfoxide (50 ml), crude crystals (7.5 g) of ethyl 6-methyl-2-(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 (50 ml), 18% hydrochloric acid (70 ml) and tin(II) chlorihe.dihydrate (16 g), ethyl 2-(2-aminoanilino)-6-methylbenzo[b]thiophene-3-carboxylate (3.7 g) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06271225B1
Source datasetuspto-grants-2001_08
ORD IDord-25e82fd7efdf443e972511b6509aa9e0
Source noteuspto-grants-2001_08