Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Cyanopyrimidine | HCID 2757979 | — |
| Edukt | Chloroform methanol | HCID 21584188 | — |
| Edukt | HCID 178418573 | HCID 178418573 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 1-(Pyrimidin-2-yl)ethan-1-one | HCID 11607909 | 48% |
Reaktionsschritte
A solution of 2-cyano-pyrimidine (10.0 g, 95.2 mmol) in THF (100 mL) was cooled to −5° C. and treated with a 3 M solution of methyl magnesium bromide in THF (38.0 mL, 98.4 mmol). The reaction was stirred at 0° C. for two hours until completion was observed by TLC (chloroform/methanol, 9:1). The reaction mixture was poured in water; the pH was adjusted to 5-6 and the aqueous layer was extracted with ethyl acetate (3×150 mL). The combined organic layers were concentrated under reduced pressure and the crude compound was purified by column chromatography, eluting with chloroform to afford the target compound (6.5 g, 48%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09249130B2 |
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| Quelldatensatz | uspto-grants-2016_02 |
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| ORD ID | ord-d8c27fd5f929441ba6aa92c44e48b9aa |
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| Quellennotiz | uspto-grants-2016_02 |
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