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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354054Generated: November 1, 2026

Stannous chloride dihydrate → Methyl 7-aminobenzofuran-4-carboxylate

https://huagongshe.com/reaction/354054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantStannous chloride dihydrateHCID 61436—
ReactantMethyl 7-nitrobenzofuran-4-carboxylateHCID 20738655—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductMethyl 7-aminobenzofuran-4-carboxylateHCID 1493932088.1%

Reaction Steps

Tin (II) chloride dihydrate (15.0 g, 66.5 mmol) was added to a suspension of 7-nitro-benzofuran-4-carboxylic acid methyl ester (4.82 g, 21.8 mmol) in ethyl acetate (80 mL) and ethanol (80 mL). The reaction mixture was stirred at room temperature for four days then partitioned between ethyl acetate and saturated aqueous solution of potassium carbonate. The organic extract was washed with brine, dried (anhydrous sodium sulfate) and concentrated under reduced pressure. The residue was purified by flash column chromatography over silica gel eluting with 30% ethyl acetate in hexane give 7-amino-benzofuran-4-carboxylic acid methyl ester (3.67 g, 88%). 1H NMR (CDCl3) δ: 3.92 (s, 3H), 6.60 (d, 1H, J=8.2 Hz), 7.34 (d, 1H, J=2.1 Hz), 7.67 (d, 1H, J=2.1 Hz), 7.84 (d, 1H, J=8.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06756395B2
Source datasetuspto-grants-2004_06
ORD IDord-552ff75ebe944761a6c6c026da337dcb
Source noteuspto-grants-2004_06