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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174699Generated: October 30, 2026

Triphenylamine → 4-Bromotriphenylamine

https://huagongshe.com/reaction/2174699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylamineHCID 11775—
ReactantN-bromobutanimideHCID 67184—
SolventEthyl AcetateHCID 8857—
Product4-BromotriphenylamineHCID 642838—

Reaction Steps

In a 1-L Erlenmeyer flask, 25 g (100 mmol) of triphenylamine, 18 g (100 mmol) of N-bromosuccinimide, and 400 mL of ethyl acetate were put and stirred at room temperature in air for 24 hours. After the reaction, the reaction solution was washed twice with a saturated aqueous solution of sodium carbonate to separate into an aqueous layer and an organic layer. The aqueous layer was extracted twice with ethyl acetate and washed with saturated saline together with the organic layer. After the organic layer was dried with magnesium sulfate, natural filtration and enrichment was performed, and the resulting white solid was recrystallized with ethyl acetate and hexane, whereby 22 g of a white powder solid of 4-bromotriphenylamine was obtained at a yield of 66%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062036B2
Source datasetuspto-grants-2015_06
ORD IDord-1b9d151aa000472b8249ca13e294ae6e
Source noteuspto-grants-2015_06