HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 889800Generated: October 25, 2026
2,4-Dimethylaniline → HCID 11424383, compound
https://huagongshe.com/reaction/889800
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dimethylaniline | HCID 7250 | — |
| Reactant | 4-Bromotoluene | HCID 7805 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 178454901 | HCID 178454901 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 11424383 | HCID 11424383 | — |
Reaction Steps
Into a 1 liter three-necked reaction vessel fitted with a cooling tube and a mechanical stirrer, 133 g (1.1 mols) of 2,4-dimethylphenylamine, 171 g (1.0 mol) of 1-bromo-4-methylbenzene, 11.2 g (0.05 mol) of palladium acetate, 32.4 g (0.2 mol) of 2-tert-butylphosphinoyl-2-methylpropane, 212 g (1.0 mol) of tripotassium phosphate and 500 mL of dimethylformamide were introduced to effect reflux for 12 hours in a nitrogen gas atmosphere and with heating in an oil bath. After the reaction was completed, the reaction mixture was left to cool to room temperature, followed by extraction with toluene/water, then washing with hydrochloric acid water, and thereafter distillation of the organic layer under reduced pressure to obtain the desired (2,4-dimethylphenyl)-p-tolylamine. The compound obtained was in a yield of 189.5 g corresponding to 84%. The compound obtained was measured with the same elementary analyzer as the above.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06994941B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-326ee85d88054ed6b1b9c4e551b60e29 |
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| Source note | uspto-grants-2006_02 |
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