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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 634534Generated: October 29, 2026

Triphenylamine → 4-Bromotriphenylamine

https://huagongshe.com/reaction/634534

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylamineHCID 11775—
ReactantN-bromobutanimideHCID 67184—
SolventEthyl AcetateHCID 8857—
Product4-BromotriphenylamineHCID 64283867.9%

Reaction Steps

25 g (100 mmol) of triphenylamine, 18 g (100 mmol) of N-bromosuccinimide, and 400 mL of ethyl acetate were put into a 1000 mL Erlenmeyer flask, and were stirred for approximately 12 hours at the room temperature in the air to be reacted. After the reaction was completed, the reaction solution was washed twice with a saturated sodium carbonate solution to separate an aqueous layer and an organic layer. Then, the aqueous layer was extracted twice with ethyl acetate, and the extract was combined with the organic layer, and washed with a saturated saline solution. The solution was dried with magnesium sulfate, and then filtration was performed. The filtrate was concentrated, and an obtained solid of 4-bromotriphenylamine was re-crystallized with ethyl acetate and hexane, whereby 22 g of a white powder solid was obtained in the yield of 66% (Synthesis Scheme (i-1)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09324951B2
Source datasetuspto-grants-2016_04
ORD IDord-eeb0b9fb3fb3456684bfd4bc68ed4b3f
Source noteuspto-grants-2016_04