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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378853Generated: October 31, 2026

Ethanol → 2-Methyl-5-benzofuranamine

https://huagongshe.com/reaction/378853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantAmmonium formateHCID 2723923—
Reactant2-Methyl-5-nitrobenzofuranHCID 4487453—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product2-Methyl-5-benzofuranamineHCID 3157484—

Reaction Steps

To a 35° C. mixture of 50 g of 2-methyl-5-nitrobenzofuran, ethanol (250 mL), THF (250 mL) and wet 10% Pd/C (4 g) was added ammonium formate (53.4 g, 0.85 mol) over 50 min. After an additional 4 h, the reaction was cooled to room temperature and filtered through Celite. The filtrate was concentrated and the residue was taken up in methyl t-butyl ether. This mixture was filtered, concentrated and dried to provide 2-methyl-5-benzofuranamine which was converted to its hydrochloride salt or its oxalate salt. The oxalate was prepared as follows: To a solution of 2-methyl-5-benzofuranamine in TBME (415 mL) was added a solution of oxalic acid (25.4 g) in methanol (80 mL) dropwise. The precipitate was stirred for 2 h, collected, washed with methanol/TBME and dried to provide 2-methyl-5-benzofuranamine oxalate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297233B1
Source datasetuspto-grants-2001_10
ORD IDord-4ffb5ed6f703406281c914226a9a8566
Source noteuspto-grants-2001_10