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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660965Generated: October 30, 2026

4-Aminophenylacetic acid → HCID 67021624, compound

https://huagongshe.com/reaction/1660965

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminophenylacetic acidHCID 14533—
Reactant1-Fluoro-2-nitrobenzeneHCID 73895—
ReactantPotassium FluorideHCID 522689—
ProductHCID 67021624HCID 67021624—

Reaction Conditions

Temperature170 °C

Reaction Steps

A mixture of 2-nitrofluorobenzene (1.5 mL, 14.2 mmol, 1.5 equiv) (Aldrich), 4-aminophenyl acetic acid (1.44 g, 9.5 mmol), and KF (0.550 g, 9.5 mmol) is stirred at 170° C. for 16 h in a sealed tube. The reaction mixture is then allowed to cool to rt, triturated in CH2Cl2/MeOH (95:5) and filtered, and the filtrate is concentrated. The residue is purified by silica gel column chromatography (CH2Cl2/MeOH, 97:3→95:5) to provide the title compound as a red solid: ES-MS: 273.0 [M+H]+; single peak at tR=4.44 min (System 1); Rf=0.20 (CH2Cl2/MeOH, 95:5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030311B2
Source datasetuspto-grants-2011_10
ORD IDord-8ca2a94d7e9344c6ba77a4cba711b611
Source noteuspto-grants-2011_10