Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl Acrylate | HCID 7294 | — |
| Edukt | Quinuclidine | HCID 7527 | — |
| Edukt | HCID 89863093 | HCID 89863093 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 89851376 | HCID 89851376 | 65% |
Reaktionsschritte
To a solution of (S)-tert-butyl 1-methoxybut-3-en-2-yl(2-oxoethyl)carbamate (Intermediate 252, 1.475 g, 6.06 mmol) and methyl acrylate (0.82 ml, 9.09 mmol) in MeOH (0.2 ml) under nitrogen at room temperature was added quinuclidine (0.337 g, 3.03 mmol). The reaction mixture was stirred at that temperature overnight. Another 100 mg of quinuclidine was added and the reaction was stirred for another 24 hours. The reaction mixture was then partitioned between water and ethyl acetate. The layers were separated and the organics were washed with water and brine, then dried over magnesium sulfate, filtered and concentrated. Silica gel chromatography (0%-30% ethyl acetate/hexanes) afforded the title compound as a clear oil (1.28 g, 65%). The product is a mixture of two diastereomers.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09309245B2 |
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| Quelldatensatz | uspto-grants-2016_04 |
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| ORD ID | ord-e080e644243f4d5097cb3905e31e5222 |
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| Quellennotiz | uspto-grants-2016_04 |
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