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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 50462Generated: October 23, 2026

Toluene → N,N'-dianisyl-1,4-phenylenediamine

https://huagongshe.com/en/reaction/50462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-BromoanisoleHCID 7730—
ReactantP-PhenylenediamineHCID 7814—
ReactantHexaneHCID 8058—
ReactantSodium t-butoxideHCID 23676156—
CatalystFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
ProductN,N'-dianisyl-1,4-phenylenediamineHCID 2130160672%

Reaction Conditions

Temperature90 °C

Reaction Steps

A flame-dried one liter three neck round bottom flask was charged with 4-bromoanisole (50.4 g, 0.26 mole), 1,4-phenylenediamine (12.0 g, 0.11 mole), 1,1 ′-bis(diphenylphosphino)ferrocene (1.776 g, 0.0032 mole), tris(dibenzylideneacetone)dipalladium(0) (0.98 g, 0.001 mole), sodium tert-butoxide (31.2 g, 0.32 mole), and anhydrous toluene (350 ml). The reaction mixture was heated to 90° C. for 48 hours. The reaction mixture was cooled to room temperature and hexane (400 ml) was added. The solid was filtered and dissolved in ethanol (400 ml). Sodium dithionite (20.0 g) was dissolved in 300 ml water and added to the ethanol solution. This was heated to reflux for 30 minutes. After the solution was cooled to room temperature, the solid was filtered off and washed with water to give 25.7 g (72%) of N,N′-dianisyl-1,4-phenylenediamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710906B2
Source datasetuspto-grants-2004_03
ORD IDord-361d3f1358d749a78e0447ed25911790
Source noteuspto-grants-2004_03