HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269524Generated: November 1, 2026
1,2-Dibromobenzene → HCID 46867078, compound
https://huagongshe.com/reaction/269524
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dibromobenzene | HCID 11414 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Acetylphenylboronic acid | HCID 2734310 | — |
| Reactant | Toluene ethanol | HCID 21863594 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 46867078 | HCID 46867078 | 63.2% |
Reaction Steps
A mixture of 3-acetylphenylboronic acid (1.64 g, 10 mmol), 1,2-dibromobenzene (4.72 g, 20 mmol), potassium carbonate (6.9 g, 50 mmol) and tetrakis(triphenylphosphine)palladium(0) (0.58 g, 0.5 mmol) in 1:1 toluene/ethanol (40 ml) was stirred and heated at 90° C. under nitrogen for 16 hours. After cooling the mixture was diluted with diethyl ether and water and the organic phase dried (MgSO4) and evaporated to dryness. The residue was purified by chromatography using Biotage with iso-hexane containing a gradient of dichloromethane (20-50%) to yield the title compound as a white solid (1.74 g 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446222B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-70c133058d284e82a4e3505a53d897a5 |
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| Source note | uspto-grants-2008_11 |
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