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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401888Generated: November 2, 2026

4-Aminobenzoic Acid → 4-(4-Methyl-2-benzoxazolyl)benzenamine

https://huagongshe.com/reaction/1401888

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminobenzoic AcidHCID 978—
Reactant2-Amino-m-cresolHCID 3014138—
Product4-(4-Methyl-2-benzoxazolyl)benzenamineHCID 5028705—

Reaction Conditions

Temperature160 °C

Reaction Steps

To a suspension of 4-amino-benzoic acid (2.0 g, 14.5 mmol) in PPA (˜85 g) was added 2-amino-m-cresol (1.8 g, 15.3 mmol). The reaction was heated to 160° C. for 14 h, then carefully quenched in aqueous sodium carbonate (˜50% saturated) at room temperature. Ethyl acetate was added, and the organic layer was washed with water and brine, and dried over sodium sulfate. The crude product was obtained was subsequently purified by flash column chromatography on silica gel eluting with ethyl acetate in hexanes to afford the desired product, 4-(4-methyl-benzooxazol-2-yl)-phenylamine as a light pink solid, 1.8 g (56%). LC-MS m/z=225 [C14H12N2O+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907103B2
Source datasetuspto-grants-2014_12
ORD IDord-5fef8a861f47485e81237a1d3bfa6666
Source noteuspto-grants-2014_12