HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227209Generated: October 30, 2026
Diethyl Ether → 4-Methyl-2-phenylpyridine
https://huagongshe.com/reaction/227209
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Bromobenzene | HCID 7961 | — |
| Reactant | 4-Methylpyridine | HCID 7963 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Sodium chloride; water | HCID 57417360 | — |
| Product | 4-Methyl-2-phenylpyridine | HCID 77026 | 36% |
Reaction Steps
A two necked round-bottom flask (250 mL) containing a stir bar fitted with a reflux condenser was evacuated and purged with nitrogen gas. Dry ether (50 mL) and bromobenzene (0.0191 mol, 3.0 g) were added to the flask followed by the slow addition of n-BuLi (0.0229 mol, 9.17 mL) via a syringe pump. The reaction mixture was stirred at room temperature for 30-40 min and then 4-methyl pyridine (0.0191 mol, 1.779 g) was slowly added. The reaction mixture was then refluxed for 2 to 3 hr. The reaction mixture was then cooled to room temperature, diluted with an aqueous brine solution and extracted with ether (3×30 mL). The combined extracts were dried over magnesium sulfate and concentrated under reduced pressure. The residue was purified by column chromatography using hexanes/EA as eluent. The desired 4-methyl-2-phenylpyridine was obtained. (1.15 g; 36% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560176B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-f7b6e2a49fc44b1dab08cc84e36abd87 |
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| Source note | uspto-grants-2009_07 |
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