HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 926418Generated: October 26, 2026
Silane, (4-bromophenyl)trimethyl- → 4-phenyl-2,5-difluoro-N-(4-trimethylsilylphenyl)benzenamine
https://huagongshe.com/reaction/926418
Participants
| Role | Name | HCID | Charge |
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| Reactant | Silane, (4-bromophenyl)trimethyl- | HCID 138897 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 4-Phenyl-2,5-difluoroaniline | HCID 46314621 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-phenyl-2,5-difluoro-N-(4-trimethylsilylphenyl)benzenamine | HCID 58099231 | 73.6% |
Reaction Steps
4-phenyl-2,5-difluoroaniline (12 mmol), 4-bromo-trimethylsilylbenzene (10 mmol), tris(dibenzylideneacetone)dipalladium(0) (0.15 mmol), (±)-2,2′-bis(diphenylphosphine)-1,1′-binaphthalene (0.3 mmol) and sodium tert-butoxie (14 mmol) are put in a two-neck round-bottom flask and dissolved in toluene (30 mL). Subsequently, the resulting solution is stirred in a bath under a temperature of about 100° C. for 24 hours. After completion of the reaction, toluene is removed. The reaction mixture is extracted with dichloromethane and water, and then being distilled under reduced pressure. The resulting residence is filtered by silica gel column and distilled under reduced pressure again. Next, by re-crystallizing and filtering with dichloromethane and petroleum ether, 4-phenyl-2,5-difluoro-N-(4-trimethylsilylphenyl)benzenamine (2.6 g) is yielded.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09284486B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-3d2a849917d6437193f10944d561968b |
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| Source note | uspto-grants-2016_03 |
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