HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402204Generated: October 30, 2026
2-Aminobiphenyl → HCID 13087228, compound
https://huagongshe.com/reaction/402204
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Aminobiphenyl | HCID 7015 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | sodium 2-methylpropan-2-olate | HCID 178418730 | — |
| Catalyst | Tris(1,1-dimethylethyl)phosphine | HCID 83681 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13087228 | HCID 13087228 | 95.4% |
Reaction Steps
Trisdibenzylideneacetonedipalladium (0.276 g, 0.3 mmol) and tri-tert-butylphosphine (0.121 g, 0.6 mmol) were put into a flask, and then dissolved in 40 mL of toluene. Subsequently, 2-biphenylamine (2.53 g, 15 mmol), bromobenzene (2.36 g, 15 mmol) and tert-butoxy sodium (2.16 g, 22.5 mmol) were added into the flask, and then refluxed at a temperature of 110° C. for 12 hours. After cooling the flask including the reactant mixture to room temperature, the reactant mixture was washed using an ammonium chloride aqueous solution (150 mL) to separate an organic layer. The separated organic layer was washed with distilled water three times, and was then dried with magnesium sulfate. Thereafter, residues from which volatile components were removed at reduced pressure were purified using a silica gel chromatography tube in a mixed solvent of hexane and ethylacetate (1:10) to produce 3.51 g of colorless N-phenylbiphenyl-2-amine liquid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08742043B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-5b4ddf61dd5f4df5a70cb8348e8fcbb5 |
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| Source note | uspto-grants-2014_06 |
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