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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1873937Erstellt: 26. Oktober 2026

1-Bromo-4-iodobenzene → N,N-bis(4-bromophenyl)-N',N'-dipheny-1,4-phenylenediamine

https://huagongshe.com/reaction/1873937

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromo-4-iodobenzeneHCID 11522—
EduktN,N-Diphenyl-p-phenylenediamineHCID 75371—
EduktSodium t-butoxideHCID 23676156—
KatalysatorFerrocene-1,1'-bis-(diphenylphosphine)HCID 635956—
Katalysator(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
LösungsmittelTolueneHCID 1140—
ProduktN,N-bis(4-bromophenyl)-N',N'-dipheny-1,4-phenylenediamineHCID 2260505661%

Reaktionsschritte

First, 27.2 mmol of 1-bromo-4-iodobenzene, 13.6 mmol of 4-Amino triphenylamine, 0.27 mmol of bis(dibenzylideneacetone)palladium ([Pd(dba)2]), 0.54 mmol of 1,1′-bis(diphenylphosphino)ferrocene (DPPF), 40.8 mmol of sodium tert-butoxide and 18 ml toluene were added into a 250 ml bottle. After heating to reflux under a nitrogen atmosphere for 6 hrs, the solvent was removed under reduced pressure, and the residue was extracted with dichloromethane/water. The collected organic layer was dried by MgSO4 overnight and then filtered to remove MgSO4. After removing the solvent of filtrate, the residue was purified by silica gel column chromatography (dichloromethane:n-hexane=1:3) and recrystallized from hexane to obtain N,N-bis(4-bromophenyl)-N′,N′-dipheny-1,4-phenylenediamine (DTPADBR) as white crystals (61% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08304514B2
Quelldatensatzuspto-grants-2012_11
ORD IDord-65a0fd4a93674b8983961bcc0f2b9c26
Quellennotizuspto-grants-2012_11