HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338192Generated: October 28, 2026
Potassium Carbonate → HCID 66813837, compound
https://huagongshe.com/reaction/338192
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Bromo-4-(tert-butyl)aniline | HCID 238591 | — |
| Reactant | (3-tert-Butylphenyl)boronic acid | HCID 21582509 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 66813837 | HCID 66813837 | 57% |
Reaction Steps
Added together were 3-t-butylphenylboronic acid (4.0 g, 22.4 mmol), 2-bromo-4-t-butyl aniline (4.3 g, 18.7 mmol), palladium(II)acetate (0.11 g, 0.468 mmol), triphenyl phosphine (0.5 g, 1.8 mmol), and 25 mL of a 2 M solution of potassium carbonate in 36 mL of ethylene glycol dimethyl ether. The reaction mixture was heated at reflux for 18 hours. The reaction was cooled to room temperature and the aqueous phase was separated from the organic phase. The aqueous phase was extracted with ethyl acetate. The organic extractions were combined, dried over magnesium sulfate filtered and concentrated. The crude product was purified by column chromatography using 20% ethyl acetate and hexanes as the eluants. The pure product 2-amino-3′,5-di-tert-butyl biphenyl (3.0 g, 57% yield) was collected as a white solid whose NMR was consistent with the proposed structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889864B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-c772857e42cd485fb67aedb7164ed9d4 |
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| Source note | uspto-grants-2014_11 |
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