HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269582Generated: October 27, 2026
Diethyl Ether → 3-(2-Bromophenyl)-5-chloro-2-(benzyloxy)pyridine
https://huagongshe.com/reaction/269582
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Bromophenyl)boronic acid | HCID 2773294 | — |
| Reactant | 2-(Benzyloxy)-3-bromo-5-chloropyridine | HCID 22058382 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene ethanol | HCID 21863594 | — |
| Product | 3-(2-Bromophenyl)-5-chloro-2-(benzyloxy)pyridine | HCID 58730997 | 42.7% |
Reaction Steps
2-(Benzyloxy)-3-bromo-5-chloropyridine (150 mg, 0.5 mmol) and 2-bromophenylboronic acid (100 mg, 0.5 mmol) were dissolved in toluene/ethanol (1:1, 5 ml) under nitrogen. Potassium carbonate (550 mg, 4 mmol) was added, followed by tetrakis(triphenylphosphine)palladium(0) (58 mg, 0.05 mmol). The resulting mixture was heated at 70° C. in a Smithcreator® microwave for 10 minutes. After cooling, diethyl ether(10 ml) and water (10 ml) were added, The organic layer was washed with water, dried (MgSO4) and evaporated. The product was purified by flash chromatography (silica gel, 2% ethyl acetate:isohexane) to give the title compound as a clear oil (80 mg).
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-0619a99b59864bf8a00077c1d42ed192 |
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| Source note | uspto-grants-2008_11 |
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