HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75073Generated: October 25, 2026
Potassium Carbonate → 2,4-Diphenylaniline
https://huagongshe.com/reaction/75073
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4-Dibromoaniline | HCID 12004 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2,4-Diphenylaniline | HCID 12316638 | 163.1% |
Reaction Steps
2,4-dibromoaniline (10 mmol), benzeneboronic acid (24 mmol), tetrakis(triphenylphosphine)palladium(0) (1 mmol) and potassium carbonate (12 g) are put in a two-neck round-bottom flask and dissolved in toluene (30 mL) and H2O (10 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, 2,4-diphenylaniline (2.0 g) is yielded.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835020B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-8b5da7c99c7443219ca237e017646c49 |
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| Source note | uspto-grants-2014_09 |
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