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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814723Generated: October 30, 2026

4-Bromoanisole → 4-Methoxytriphenylamine

https://huagongshe.com/reaction/1814723

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromoanisoleHCID 7730—
ReactantDiphenylamineHCID 11487—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
Reactantsodium 2-methylpropan-2-olateHCID 178418730—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product4-MethoxytriphenylamineHCID 988203770%

Reaction Conditions

Temperature100 °C

Reaction Steps

10 g of diphenylamine and 11 g of 4-methoxy-bromobenzene was dissolved in toluene (250 mL). NaO-t-Bu (5.3 g), Pd2(dba)3 (0.4 g), and P(t-Bu)3 (0.5 g) were added to the above solution at room temperature. The reaction mixture was stirred at 100° C. for 12 hours under N2 After cooling to room temperature, the mixture was quenched by adding aqueous ammonia (300 mL). An organic layer was separated from the reactant solution using methylene chloride and dried using magnesium sulfate. Then, methylene chloride was removed under reduced pressure and recrystallized using methylene chloride and hexane, yielding 70% of a white solid. Data of NMR spectra and elemental analysis confirmed that the product had the same structure as the compound (6) in the reaction scheme 4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878468B2
Source datasetuspto-grants-2005_04
ORD IDord-e02309ca286546059dd4a40a9e0e3f88
Source noteuspto-grants-2005_04