HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577457Generated: October 28, 2026
Benzyl Chloride → HCID 86723689, compound
https://huagongshe.com/reaction/577457
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Chloride | HCID 7503 | — |
| Reactant | 4-Ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile | HCID 15641800 | — |
| Catalyst | HCID 178418778 | HCID 178418778 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86723689 | HCID 86723689 | 83% |
Reaction Steps
A mixture of 4-ethyl-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile (Cpd AA, 1.1 g, 6.8 mmol), (chloromethyl)benzene (1.1 mL, 9.4 mmol, 1.4 equiv) and silver(I) oxide (1.8 g, 7.7 mmol) in anhydrous toluene (22.7 mL) was heated at 110° C. for 17 hours. The reaction mixture was cooled to 23° C. then filtered through CELITE®. The filtrate was concentrated under vacuum. The residue was purified by column chromatography (heptane/EtOAc) to give 2-(benzyloxy)-4-ethyl-6-methylpyridine-3-carbonitrile (Cpd BB, 1.42 g, 83%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040515B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-45fbec9cd137473fb3784c556afecee3 |
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| Source note | uspto-grants-2015_05 |
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