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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173349Generated: October 29, 2026

Ethyl 6-amino-1-benzofuran-3-carboxylate → HCID 67516008, compound

https://huagongshe.com/reaction/2173349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 6-amino-1-benzofuran-3-carboxylateHCID 67515639—
SolventMethanolHCID 887—
ProductHCID 67516008HCID 67516008—

Reaction Steps

A mixture of ethyl 6-amino-1-benzofuran-3-carboxylate (2.0 g, 9.8 mmol) in 50 mL of MeOH was added Mg filings (1.17 g, 49 mmol) ans the mixtrue was stired overnight at room temperature. The mixture was filtered and the filtrate was concentrated. The residue was then partitioned between EtOAc and water. The combined organic phase was washed with brine, dried over anhydrous sodium sulfate and concentrated. The residue was purified with silca gel column chromatograph to give methyl 6-amino-2,3-dihydro-1-benzofuran-3-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-a2b4ea049567489aa6735e0434ab510c
Source noteuspto-grants-2015_06