Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diethyl Ether | HCID 3283 | — |
| Edukt | 3-Bromopyridine | HCID 12286 | — |
| Edukt | Ethyl N-methoxy-N-methylcarbamate | HCID 533715 | — |
| Edukt | Butyllithium | HCID 178418339 | — |
| Produkt | Di-3-pyridinylmethanone | HCID 298471 | 33% |
Reaktionsschritte
To a solution of 3-bromopyridine (9.84 g, 0.062 mol) in 300 mL of ether cooled to -78° C. was added n-butyllithium (1.6M, 41 mL, 0.066 mol) and stirred for 30 min. N-Methyl,N-methoxy-urethane (3.76 g, 0.028 mol) in 20 mL of ether was added in 10 min, the mixture was stirred (-78° C.) for 1 h, allowed to warm to room temperature and stirred for 2 h. The reaction mixture was quenched with 6N HCl (100 mL) and stirred. The aqueous layer was basified with 10% NaOH solution, extracted with ethyl acetate (2×) and methylene dichloride. The organic layer was dried over sodium sulfate, concentrated in vacuo, and the residue was purified by chromatography on silica (ethyl acetate, 10% methanol/ethyl acetate) to afford 1.7 g (33%) of di-(3-pyridyl)ketone.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05554620 |
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| Quelldatensatz | uspto-grants-1996_09 |
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| ORD ID | ord-a84c0e5983224b928786a06dc687df70 |
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| Quellennotiz | uspto-grants-1996_09 |
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