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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13910Generated: October 25, 2026

Bromobenzene → Triphenylamine

https://huagongshe.com/reaction/13910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromobenzeneHCID 7961—
ReactantDiphenylamineHCID 11487—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
CatalystDi-tert-butyl-1-naphthylphosphonium tetraphenylborateHCID 23136633—
SolventO-XyleneHCID 7237—
ProductTriphenylamineHCID 1177585%

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, 0.071 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728176B2
Source datasetuspto-grants-2010_06
ORD IDord-b7cb727e80394547aa77a6af673b056c
Source noteuspto-grants-2010_06