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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 877287Generated: October 25, 2026

Di-tert-butylchlorophosphine → 4-(Bis(3-methylphenyl)amino)benz[a]-anthracene

https://huagongshe.com/reaction/877287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDi-tert-butylchlorophosphineHCID 139566—
ReactantBenz(a)anthracene, 4-bromo-HCID 182324—
Reactantm,m'-DitolylamineHCID 7016139—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product4-(Bis(3-methylphenyl)amino)benz[a]-anthraceneHCID 59412657—

Reaction Conditions

Temperature60 °C

Reaction Steps

190 μl (1 mmol) of chloro-di-tert-butylphosphine and then 112 mg (0.5 mmol) of palladium(II) acetate are added to a suspension of 15.4 g (50 mmol) of 4-bromobenz[a]anthracene, 11.8 g (60 mmol) of bis(3-methylphenyl)amine and 7.7 g (80 mmol) of sodium tert-butoxide in 500 ml of toluene, and the mixture is subsequently heated under reflux for 5 h. After the mixture has been cooled to 60° C., 500 ml of water are added, the organic phase is separated off, filtered through silica gel, evaporated virtually to dryness at 80° C. in vacuo, and 300 ml of ethanol are then added. After cooling, the solid is filtered off with suction. Recrystallisation five times from dioxane (about 8 ml/g); sublimation (p=5×10−5 mbar, T=280° C.). Yield: 11.9 g (28 mmol), 56.1%, purity 99.9% (HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08986852B2
Source datasetuspto-grants-2015_03
ORD IDord-b725f01181bc4dc6bc9acb588e93bfa7
Source noteuspto-grants-2015_03