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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-Methoxy-N-(4-methoxyphenyl)-N-phenylaniline | HCID 10543043 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Bromo-4',4''-dimethoxytriphenylamine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846978B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-844f93307fae4200a82776709e8e9fec |
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| Source note | uspto-grants-2014_09 |
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