HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72814Generated: October 26, 2026
2-Bromotoluene → Benzenamine, 2-methyl-N-(2-methylphenyl)-
https://huagongshe.com/reaction/72814
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromotoluene | HCID 7236 | — |
| Reactant | 2-Chlorotoluene | HCID 7238 | — |
| Reactant | Lithium amide | HCID 24532 | — |
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Catalyst | (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium | HCID 6505921 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Benzenamine, 2-methyl-N-(2-methylphenyl)- | HCID 136423 | 72% |
Reaction Steps
The round-bottom flask was heated then allow to cool to room temperature under argon. Added Pd2(dba)3 (1.39 g, 1.52 mmol, 1.0 mol %) or Pd(dba)2 (1.38 g, 2.4 mmol, 1.4 mol %), 2-(di-tert-butylphosphino)biphenyl (1.09 g, 3.65 mmol, 2.4 mol %), 2-bromotoluene (40 mL, 332.1 mmol) or 2-chlorotoluene (39 mL, 332.1 mmol), lithium amide (3.47 g, 151.1 mmol, 45 mol %), sodium t-butoxide (29.5 g, 297.7 mmol, 90 mol %), followed by toluene (150 mL). The reaction mixture was heated at 80° C. under argon overnight, then allowed to cool to room temperature. Diluted with diethyl ether then filtered through a pad of Celite. Concentrated the resulting filtrate in vacuo. Used the crude material in the next reaction without purification. (Crude material can be purified by flash chromatography with hexane which gave the product as white crystals with a yellow tint (23.4 g, 118.6 mmol, 72% yield)).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828986B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-6dc0c40063fa4ce2bed62a222591a84e |
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| Source note | uspto-grants-2014_09 |
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