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HRID 394823Erstellt: 24. Oktober 2026

N,N'-Diphenyl-P-Phenylenediamine → N,N'-Diphenyl-N,N'-di(m-tolyl)-1,4-phenylenediamine

https://huagongshe.com/de/reaction/394823

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN,N'-Diphenyl-P-PhenylenediamineHCID 6319—
Edukt(+-)-alpha-PineneHCID 6654—
Edukt3-IodotolueneHCID 12268—
Eduktsodium 2-methylpropan-2-olateHCID 178418730—
KatalysatorCuprous chlorideHCID 62652—
Katalysator2-(5,6-Diphenyl-2-pyridyl)pyridineHCID 9861424—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
ProduktN,N'-Diphenyl-N,N'-di(m-tolyl)-1,4-phenylenediamineHCID 1425051890,5%

Reaktionsschritte

A mixture of 31.2 g (0.12 mole) of N,N′-diphenyl-N,N′-p-phenylenediamine, 54.5 g (0.25 mole) of m-iodotoluene, 32.6 g (0.34 mole) of t-butoxy sodium, 59.0 mg (0.6 mmole) of copper (I) chloride, 185 mg (0.6 mmole) of 2-(5,6-diphenyl-2-pyridyl)pyridine (A-8) and 87.6 ml of α-pinene was reacted at 125 to 130° C. for 5 hours under a nitrogen gas stream. After completion of the reaction, 66 ml of toluene and 66 ml of water were added to separate the reaction mixture. Toluene was then concentrated under reduced pressure. The residue was crystallized by the addition of 39 ml of ethyl acetate and 253 ml of isopropanol, whereby 47.8 g (yield: 90.5%) of the target compound was obtained as pale yellow crude crystals. The compound was found to have a melting point of 170 to 171° C. and an HPLC content (column: YMC-A-002, UV detector: 310 nm, eluent having a flow rate of 1.1 ml/min) was 99.5%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06603007B1
Quelldatensatzuspto-grants-2003_08
ORD IDord-ec820f4221474c6e9e960e66d32ab375
Quellennotizuspto-grants-2003_08