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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1844102Generated: October 31, 2026

2,4-Dinitrophenylacetic acid → 2-(2,4-diaminophenyl)acetic acid

https://huagongshe.com/reaction/1844102

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dinitrophenylacetic acidHCID 221513—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-(2,4-diaminophenyl)acetic acidHCID 226262—

Reaction Steps

To 2,4-dinitrophenylacetic acid (1.2 gm) in methanol (60 mL), added Pd/C (80 mg, 10 wt %). H2 gas environment was maintained with pressure using hydrogen gas balloon and solution stirred for 6 hours at RT. The catalyst was removed by filtration, over celite. The filtrate was concentrated in vacuo to give 2,4-diaminophenylacetic acid without further purification, immediately refluxed with 16 ml of 1N HCl for 6 hrs. Reaction was monitored with TLC. The solution was neutralized with 1% sodium hydroxide, extracted with three portions of ethyl acetate. The organic layers were combined, dried over anhydrous sodium sulfate or magnesium sulfate, evaporated in vacuo to get the title compound D4: YD: 67.85%: mp: 193-195° C.; Rf: 0.358 (EA:Hx: 7.0:3.0). 1H NMR (DMSO-d6) 200 MHz, δ: 3.227 (s, 2H), 5.004 (s, 2H) —NH2, 6.094 (dd, J=2.2 & 6.2 Hz, 1H), 6.098 (d, J=2.0 Hz, 1H), 6.786 (d, J=8.4 Hz, 1H), 10.088 (s, 1H). MS (ESI): m/z 146.8 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946282B2
Source datasetuspto-grants-2015_02
ORD IDord-ca20af4b0c504da9935d3998624666f0
Source noteuspto-grants-2015_02