HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 38081Erstellt: 25. Oktober 2026
4-Methylpyridine → 1-(3-Methoxyphenyl)-2-(4-pyridyl)ethanone
https://huagongshe.com/reaction/38081
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Methylpyridine | HCID 7963 | — |
| Edukt | Ammonium Chloride | HCID 25517 | — |
| Edukt | Methyl 3-methoxybenzoate | HCID 79332 | — |
| Edukt | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(3-Methoxyphenyl)-2-(4-pyridyl)ethanone | HCID 11276228 | 71,7% |
Reaktionsschritte
To a solution of 4-methyl-pyridine (1.04 mL, 10.74 mmol) in anhydrous tetrahydrofuran (40 mL) at 0° C. a 1 M solution of sodium hexamethyldisilazide in tetrahydrofuran (21.5 mL, 21.5 mmol, 2 eq) was added dropwise and the reaction was stirred for 20 minutes. Neat methyl 3-methoxybenzoate (1.8 g, 10.74 mmol, 1 eq) was then added and the reaction was stirred at 0° C. for one hour. The reaction was poured into saturated ammonium chloride solution and, after basification with saturated aqueous NaHCO3, extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The crude product was taken up with n-hexane and filtered to give 1.75 g (72%) of the desired product as beige solid (1.775 g, 50%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08524707B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-6d51969d966040b2b5589d90636798f0 |
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| Quellennotiz | uspto-grants-2013_09 |
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