HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193022Generated: October 31, 2026
4-Bromobenzaldehyde → HCID 59327809, compound
https://huagongshe.com/reaction/1193022
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Bromobenzaldehyde | HCID 70741 | — |
| Reactant | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 59327800 | HCID 59327800 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59327809 | HCID 59327809 | — |
Reaction Steps
4-butyl-N-(2,4-difluorophenyl)benzeneamine (30 m mol)), 4-bromobenzaldehyde (34 m mol)), tris(dibenzylideneaceton)dipalladium(O) (0.5 m mol)), tris-tert-butylphosphine (0.9 m mol)), and sodium-tert-butoxide (40 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, reduced pressure and distillation were performed on the resulting solution. After a silica gel column chromatography, the solvent was reduced in pressure and distilled, thereby obtaining 4-(N-(4-butylphenyl)-N-(2,4-difluorophenyl)amino)benzaldehyde liquid having 7.1 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-b0ee8c19858e4947ad7d6e370dc0c595 |
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| Source note | uspto-grants-2014_03 |
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