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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645725Generated: October 26, 2026

Bromobenzene → Triphenylamine

https://huagongshe.com/reaction/1645725

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 numberUS08124809B2
Source datasetuspto-grants-2012_02
ORD IDord-920353957b3945a8b0310e067b683739
Source noteuspto-grants-2012_02