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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399455Generated: October 31, 2026

2-(3-Fluoro-4-nitrobenzamido)acetic acid → 2-(4-Amino-3-fluorobenzamido)acetic acid

https://huagongshe.com/reaction/1399455

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(3-Fluoro-4-nitrobenzamido)acetic acidHCID 15925739—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
SolventEthyl AcetateHCID 8857—
Product2-(4-Amino-3-fluorobenzamido)acetic acidHCID 1592574171%

Reaction Conditions

Temperature87.5 °C

Reaction Steps

To a suspension of iron powder (231 mg, 4.13 mmol) in AcOH (2 mL) was added 2-(3-fluoro-4-nitrobenzamido)acetic acid (100 mg, 0.413 mmol) at rt and stirred at 85-90° C. for 15 min. The reaction mixture was attained to rt and diluted with EtOAc (20 mL). The solution was stirred for 5 min and filtered through celite. The celite bed was washed with EtOAc (10 mL) and the combined organic layer was evaporated under reduced pressure. The residue was chromatographed over silica gel column using chloroform:methanol (70:30) as eluents to give the product as an off-white color solid (62 mg, 71%), 198-200° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906344B2
Source datasetuspto-grants-2014_12
ORD IDord-b243069e5cc0469dbbf7a5c0767c2291
Source noteuspto-grants-2014_12