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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384351Generated: October 27, 2026

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

https://huagongshe.com/reaction/384351

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 28c (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 reaction was monitored by TLC until the disappearance of the starting materials. 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 28d (325 mg, yield 73.4%) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-1bd107c68a4f4c879c7aa67ce1039b8f
Source noteuspto-grants-2013_02