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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1912158Erstellt: 27. Oktober 2026

Bromobenzene → Triphenylamine

https://huagongshe.com/reaction/1912158

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBromobenzeneHCID 7961—
EduktDiphenylamineHCID 11487—
EduktSodium t-butoxideHCID 23676156—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorDi-tert-butyl-1-naphthylphosphonium tetraphenylborateHCID 23136633—
LösungsmittelO-XyleneHCID 7237—
ProduktTriphenylamineHCID 1177585%

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, 0.071 g (0.12 mmol) of di-tert-butyl-1-naphthylphosphonium tetraphenylborate obtained in Example B-11 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 8.341 g of triphenylamine (yield: 85 mol % based on diphenylamine). The melting point was 125-126° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08604249B2
Quelldatensatzuspto-grants-2013_12
ORD IDord-a51dc61d8bfb415a975508923d513688
Quellennotizuspto-grants-2013_12