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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1791206Generated: November 3, 2026

4-Tert-Butylaniline → (4-tert-Butyl-phenyl)-[7-(2-trifluoromethyl-phenyl)-quinolin-4-yl]-amine

https://huagongshe.com/reaction/1791206

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Tert-ButylanilineHCID 69861—
ReactantHCID 22030439HCID 22030439—
SolventIsopropanolHCID 3776—
Product(4-tert-Butyl-phenyl)-[7-(2-trifluoromethyl-phenyl)-quinolin-4-yl]-amineHCID 22030258—

Reaction Steps

Heat a mixture of 4-chloro-7-(2-trifluoromethyl-phenyl)-quinoline (42 mg, 0.14 mmol) and 4-(tert-butyl)aniline (41 mg, 0.29 mmol) in 2-propanol (10 mL) at reflux for 3 hours. Evaporate the mixture, add 1M NaOH (10 mL), extract twice with EtOAc (10 mL each), dry (Na2SO4), and evaporate to provide the crude product. Purify by silica gel chromatography, eluting with 75% hexane-EtOAc to provide (4-tert-Butyl-phenyl)-[7-(2-trifluoromethyl-phenyl)-quinolin-4-yl]-amine as a white solid. Mass spec. 420.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07074799B2
Source datasetuspto-grants-2006_07
ORD IDord-7d5f6a01c648471eabeceb164af85f3f
Source noteuspto-grants-2006_07