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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 13908Erstellt: 23. Oktober 2026

Bromobenzene → Triphenylamine

https://huagongshe.com/de/reaction/13908

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromobenzeneHCID 7961—
EduktDiphenylamineHCID 11487—
EduktSodium t-butoxideHCID 23676156—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorDi-tert-butylphenylphosphonium tetraphenylborateHCID 23136655—
LösungsmittelO-XyleneHCID 7237—
ProduktTriphenylamineHCID 1177592%

Reaktionsschritte

A 100-ml four-necked flask was equipped with a stirrer, a thermometer and a reflux condenser. 7.536 g (48 mmol) of bromobenzene, 6.769 g (40 mmol) of diphenylamine, 4.613 g (48 mmol) of sodium-tert-butoxide, 0.009 g (0.04 mmol) of palladium (II) acetate and 5 ml of xylene were weighed in the flask, followed by stirring. Further, 0.065 g (0.12 mmol) of di-tert-butylphenylphosphonium tetraphenylborate obtained in Example B-9 was weighed in air and added into the flask. The flask was purged with argon, followed by stirring at 125° C. for 4 hours. After the completion of the reaction, 45 ml of xylene and 50 ml of saturated sodium chloride solution were added, followed by separation. The organic phase was purified by column chromatography to afford 9.028 g of triphenylamine (yield: 92 mol % based on diphenylamine). The melting point was 125-126° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728176B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-679046ba82444c97a0cf79c2478c7f13
Quellennotizuspto-grants-2010_06