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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2356191Generated: October 31, 2026

Dodecane → N,N'-diphenyl-N,N'-di-p-tolyl-4,4''-diamino-p-terphenyl

https://huagongshe.com/reaction/2356191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDodecaneHCID 8182—
ReactantPotassium CarbonateHCID 11430—
ReactantN-Phenyl-p-toluidineHCID 12109—
Reactant4,4''-Diiodo-p-terphenylHCID 3563583—
CatalystCopperHCID 23978—
ProductN,N'-diphenyl-N,N'-di-p-tolyl-4,4''-diamino-p-terphenylHCID 1400824476.4%

Reaction Conditions

Temperature205 °C

Reaction Steps

Phenyl-p-tolylamine (11.5 g (0.063 mol)), 14.5 g (0.030 mol) of 4,4″-diiodo-p-terphenyl, 5.0 g (0.036 mol) of anhydrous potassium carbonate, 0.38 g (0.006 mol) of copper powder and 15 ml of n-dodecane were mixed, and heated up to 200 to 210° C. while introducing nitrogen gas, followed by stirring for 30 hours. After the termination of the reaction, the reaction product was extracted with 400 ml of toluene, and insoluble matter was removed by filtration. Then, the filtrate was concentrated to dryness. The resulting solid matter was purified by column chromatography (carrier: silica gel, eluent: toluene:hexane=1:4) to obtain 13.6 g of N,N′-diphenyl-N,N′-di-p-tolyl-4,4″-diamino-p-terphenyl (compound No. 17) (yield: 76.4%, melting point: 167.2 to 168.2° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759030B2
Source datasetuspto-grants-2010_07
ORD IDord-2f947d001eb3442abda9f12d95a7bfeb
Source noteuspto-grants-2010_07