Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84993Generated: October 27, 2026

Ethyl Acetate → 4-Bromo-4',4''-dimethoxytriphenylamine

https://huagongshe.com/reaction/84993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantN-bromobutanimideHCID 67184—
Reactant4-Methoxy-N-(4-methoxyphenyl)-N-phenylanilineHCID 10543043—
SolventDimethylformamideHCID 6228—
Product4-Bromo-4',4''-dimethoxytriphenylamineHCID 10596161—

Reaction Steps

2. N,N-bis(4-methoxyphenyl)aniline 1 (9.0 g, 29.5 mmol) was dissolved in 100 mL dimethylformamide in a 250 mL round bottom flask. N-bromosuccinimide (5.25 g, 29.5 mmol) was dissolved in 30 mL dimethylformamide and added dropwise to the reaction mixture. The reaction was allowed to stir at room temperature while being monitored by thin layer chromatography (TLC) (Reaction Time=23 h). The reaction mixture was quenched using 600 mL water and extracted with 4×150 mL dichloromethane. The organic layers were combined and washed with 4×150 mL saturated sodium thiosulfate solution and dried over sodium sulfate. The solvent was removed under reduced pressure. The product was purified along with materials prepared previously using flash chromatography on silica gel eluting with 5:1 hexanes:ethylacetate (12.1 g, 100%). 1H NMR (300 MHz, CDCl3) δ 7.28 (d, J=9.0 Hz, 2H), 7.05 (d, J=9.0 Hz, 4H), 6.90 (d, J=9.0 Hz, 4H), 6.73 (d, J=9.0 Hz, 2H), 3.77 (s, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846978B2
Source datasetuspto-grants-2014_09
ORD IDord-844f93307fae4200a82776709e8e9fec
Source noteuspto-grants-2014_09