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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912134Generated: November 1, 2026

Chlorobenzene → Triphenylamine

https://huagongshe.com/reaction/1912134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorobenzeneHCID 7964—
ReactantDiphenylamineHCID 11487—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
CatalystTri-tert-butylphosphonium TetraphenylborateHCID 23136663—
SolventO-XyleneHCID 7237—
ProductTriphenylamineHCID 1177591.8%

Reaction Steps

A 100-ml four-necked flask was equipped with a stirrer, a thermometer and a reflux condenser. 5.403 g (48 mmol) of chlorobenzene, 6.769 g (40 mmol) of diphenylamine, 4.613 g (48 mmol) of sodium-tert-butoxide, 0.002 g (0.01 mmol) of palladium (II) acetate and 5 ml of xylene were weighed in the flask, followed by stirring. Further, 0.021 g (0.04 mmol) of tri-tert-butylphosphonium tetraphenylborate obtained in Example A-1 was weighed in air and added into the flask. The flask was purged with argon, followed by stirring at 100-120° C. for 10 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 9.008 g of triphenylamine (yield: 92 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-a9122707b1824246bc9d298d9fb5f550
Source noteuspto-grants-2013_12