HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384047Generated: October 30, 2026
Isobutyronitrile → 2-(6-Bromopyridin-2-yl)-2-methylpropanenitrile
https://huagongshe.com/reaction/384047
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isobutyronitrile | HCID 6559 | — |
| Reactant | 2,6-Dibromopyridine | HCID 12274 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-(6-Bromopyridin-2-yl)-2-methylpropanenitrile | HCID 57969658 | 65.5% |
Reaction Steps
Potassium bis(trimethylsilyl)amide (0.5 M in toluene, 200 ml, 100 mmol) was added slowly to a solution of isobutyronitrile (8.55 ml, 95.26 mmol) in toluene (200 ml) cooled down to 0° C. After complete addition, the reaction mixture was allowed to warm up to room temperature over 1 hour. The resulting mixture was added to a solution of 2,6-dibromopyridine (56.42 g, 238.15 mmol) in toluene (100 ml). The reaction mixture was stirred at room temperature for 18 hours. The crude mixture was diluted with ether, washed with a saturated aqueous solution of ammonium chloride and brine. The organic phase was dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography to afford the title compound as an oil (14.04 g, 65% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367697B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-ccc80749565e4d3a8e5cc79fee5e0763 |
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| Source note | uspto-grants-2013_02 |
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