HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193021Generated: October 29, 2026
2,4-Difluoroaniline → HCID 59327800, compound
https://huagongshe.com/reaction/1193021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | 1-Bromo-4-butylbenzene | HCID 521059 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59327800 | HCID 59327800 | — |
Reaction Steps
2,4-difluoroaniline (44 m mol)), 1-bromo-4-butylbenzene (30 m mol)), palladium(II)acetate (0.4 m mol)), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.9 m mol)), and potassium-tert-butoxide (44 m mol)) were dissolved in toluene (100 ml) in a 250 ml tri-neck-round bottom flask and then stirred in a bath of 100° C. for 24 hours. After the reaction was terminated, the toluene was removed from the solution. After extraction was performed on the solution using dichloromethane and water, the resulting solution was reduced in pressure and distilled. After a silica gel column chromatography, the solvent was reduced in pressure and distilled, thereby obtaining 4-butyl-N-(2,4-difluorophenyl)benzeneamine liquid having 0.3 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08680336B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-e2d3bf22ee764bce8fd4171bf02abd16 |
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| Source note | uspto-grants-2014_03 |
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