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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1755514Erstellt: 27. Oktober 2026

Phenyl-1-naphthylamine → N-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amine

https://huagongshe.com/reaction/1755514

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenyl-1-naphthylamineHCID 7013—
Edukt4,4'-DibromobiphenylHCID 7110—
EduktSodium t-butoxideHCID 23676156—
KatalysatorBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
LösungsmittelTolueneHCID 1140—
ProduktN-(4'-bromo-[1,1'-biphenyl]-4-yl)-N-phenylnaphthalen-1-amineHCID 1675531262%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

A mixture of N-phenylnaphthalen-1-amine (4.41 g, 20 mmol), 4,4′-dibromo-1,1′-biphenyl (15 g, 48 mmol), sodium tert-butoxide (NaOBut) (4.8 g, 50 mmol) and Pd(dppf)Cl2 (0.44 g, 0.6 mmol) in anhydrous toluene (100 mL) was degassed and heated at 80° C. for about 10 hours. After cooling to RT, the mixture was poured into dichloromethane (400 mL) and stirred for about 30 min., then washed with brine (100 mL). The organic solution was collected and dried over Na2SO4, loaded on silica gel, and purified by flash column (hexanes to hexanes/ethyl acetate 90:1) to give a solid which was washed with methanol and dried under air to give a white solid Compound 4 (5.58 g, in 62% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09172051B2
Quelldatensatzuspto-grants-2015_10
ORD IDord-bb1c2452679d4f3d8feb4e1f7f9f8309
Quellennotizuspto-grants-2015_10