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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912157Generated: October 26, 2026

Bromobenzene → Triphenylamine

https://huagongshe.com/reaction/1912157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantDiphenylamineHCID 11487—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
Catalyst2-Biphenylyl-di-tert-butylphosphonium tetraphenylborateHCID 23136673—
SolventO-XyleneHCID 7237—
ProductTriphenylamineHCID 1177587%

Reaction Steps

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, 0.074 g (0.12 mmol) of 2-biphenylyl-di-tert-butylphosphonium tetraphenylborate obtained in Example B-10 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 8.537 g of triphenylamine (yield: 87 mol % based on diphenylamine). The melting point was 125-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604249B2
Source datasetuspto-grants-2013_12
ORD IDord-480a0526069a48ae84796e3cb00596e2
Source noteuspto-grants-2013_12