Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1835631Generated: November 1, 2026

N-Phenyl-p-phenylenediamine → HCID 20268565, compound

https://huagongshe.com/reaction/1835631

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Phenyl-p-phenylenediamineHCID 7564—
ReactantPhenol, 4-(bromomethyl)-2,6-bis(1,1-dimethylethyl)-HCID 612973—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20268565HCID 20268565—

Reaction Steps

4-Bromomethyl-2,6-di-tert-butyl-phenol (2.42 g, 0.008 mole) was dissolved in 50 mL of dry tetrahydrofuran . In a separate conical flask N-Phenyl-benzene-1,4-diamine (2.93 g, 0.016 mole) was dissolved in 25 mL of tetrahydrofuran and solution was transferred to a cylindrical funnel with pressure equalizing tube. Three-necked round-bottomed flask containing solution of 4-Bromomethyl-2,6-di-tert-butyl-phenol was kept in oil-bath at 85° C. Solution in the flask was continuously stirred with the help of magnetic stirrer. N-Phenyl-benzene-1,4-diamine solution was added drop-by-drop, from funnel to the flask in acidic medium for a span of 4-5 hours till all the solution was poured out. The reaction was terminated after that and the final reaction mixture was allowed to attain room temperature. Product was separated by solvent evaporation. The product was purified using silica gel column chromatography. Product was identified by 1H-NMR. The yield of 2,6-di-tert-butyl-4-[(4-phenylamino-phenylamino)phenol is 2.044 g (63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06770785B1
Source datasetuspto-grants-2004_08
ORD IDord-e88fefde1bd447b79bab170c8a890dec
Source noteuspto-grants-2004_08