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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399446Generated: October 30, 2026

Benzyl 2-(4-fluoro-3-nitrobenzamido)acetate → 2-(3-Amino-4-fluorobenzamido)acetic acid

https://huagongshe.com/reaction/1399446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 2-(4-fluoro-3-nitrobenzamido)acetateHCID 86713118—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-(3-Amino-4-fluorobenzamido)acetic acidHCID 7343783070%

Reaction Steps

To a solution of benzyl 2-(4-fluoro-3-nitrobenzamido)acetate (85 mg) in EtOAc (10 mL) was added Pd/C (10%, 100 mg) at rt and stirred under the atmosphere of H2 gas for 25 min. Work-up of the reaction mixture as described in example 1 gave the product as a white color solid (38 mg, 70%), mp 150-152° C. 1H NMR (400 MHz, CDCl3+DMSO-d6): δ 7.74 (1H, br s), 7.37 (1H, dd, J=8.6, 1.8 Hz), 7.12-7.16 (1H, m), 6.97 (1H, dd, J=10.6, 8.6 Hz), 4.07 (2H, d, J=5.6 Hz); 13C NMR (100 MHz, CDCl3+DMSO-d6): δ 170.6, 165.9, 151. 9 (d, J=242 Hz), 134.5 (d, J=13 Hz), 129.6 (d, J=3 Hz), 115.4 (d, J=8 Hz), 115.1 (d, J=6 Hz), 113.6 (d, J=19 Hz), 40.5; LC-MS (negative ion mode): m/z 211 (M−H)−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906344B2
Source datasetuspto-grants-2014_12
ORD IDord-0c95adb23b0343bda67f1ae9c4c371b0
Source noteuspto-grants-2014_12