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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271454Generated: October 27, 2026

Ammonium formate → 4-(3-Amino-2-methoxy-phenyl)-furan-2-carboxylic acid

https://huagongshe.com/reaction/2271454

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
Reactant4-(3-Nitro-2-methoxy-phenyl)-furan-2-carboxylic acidHCID 57483824—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product4-(3-Amino-2-methoxy-phenyl)-furan-2-carboxylic acidHCID 5748382573.4%

Reaction Steps

4-(3-nitro-2-methoxy-phenyl)-furan-2-carboxylic acid 22c (500 mg, 1.9 mmol) was dissolved in 15 mL of ethyl acetate followed by addition of 100 mg of palladium on carbon and ammonium formate (429 mg, 7.6 mmol). The reaction mixture was heated to reflux for 3 hours. The mixture was filtered to remove palladium on carbon and concentrated under reduced pressure to obtain the title compound 4-(3-amino-2-methoxy-phenyl)-furan-2-carboxylic acid 22d (325 mg, yield 73.4%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09120762B2
Source datasetuspto-grants-2015_09
ORD IDord-5ac69ad0a03249ffa856d32d010b75f7
Source noteuspto-grants-2015_09