HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 72288Generated: October 25, 2026
Potassium Carbonate → N-(4'-chloro-3-ethylbiphen-4-yl)acetamide
https://huagongshe.com/reaction/72288
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chlorophenylboronic acid | HCID 74299 | — |
| Reactant | N-(4-bromo-2-ethylphenyl)acetamide | HCID 2735223 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(4'-chloro-3-ethylbiphen-4-yl)acetamide | HCID 59450487 | 91.3% |
Reaction Steps
To a degassed solution of N-(4-bromo-2-ethylphenyl)acetamide (20 g, 0.082 mol) in toluene (1200 ml) and ethanol (400 ml), 4-chlorobenzene boronic acid (15.5 g, 0.099 mol) is added under an atmosphere of nitrogen, and the reaction mixture is heated to 80° C. Tetrakis(triphenylphosphine)palladium(0) (2.0 g, 0.0017 mol) is added followed by 2M aqueous potassium carbonate solution (160 ml). The reaction mixture is heated at reflux for 4 hours then cooled to room temperature. The reaction mixture is filtered through diatomaceous earth, and the filtrate is evaporated under reduced pressure. The residue is partitioned between ethyl acetate and water. The aqueous phase is extracted with ethyl acetate (3×500 ml) and the organic solutions are combined and concentrated under reduced pressure to give N-(4′-chloro-3-ethylbiphen-4-yl)acetamide (20.5 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08828908B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-a0c1abc68792466d9fe31d229cb7b1a5 |
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| Source note | uspto-grants-2014_09 |
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