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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010722Generated: October 30, 2026

4-Aminophenylacetic acid → HCID 67021624, compound

https://huagongshe.com/reaction/1010722

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 1.5 ml of 2-nitrofluorobenzene (Aldrich), 1.44 g of 4-aminophenyl acetic acid and 0.550 g of KF is stirred at 170° C. for 16 hours in a sealed tube. The mixture obtained is allowed to cool to rt, triturated in CH2Cl2/MeOH (95:5) and filtered. The filtrate obtained is concentrated and the concentrate obtained is purified by silica gel column chromatography. [4-(2-Nitro-phenylamino)-phenyl]-acetic acid is obtained in the form of a 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 numberUS07977338B2
Source datasetuspto-grants-2011_07
ORD IDord-ee93fe5c6c454020964361fb7fd60282
Source noteuspto-grants-2011_07