Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Trimethylsulfonium methyl sulfate | HCID 2760871 | — |
| Katalysator | Tetrabutylammonium Bromide | HCID 74236 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | 3-(Oxiran-2-yl)pyridine | HCID 13319561 | 28,6% |
Reaktionsschritte
To a solution of 2.59 g of 3-pyridinecarboxaldehyde and 62 mg of tetra-n-butylammonium bromide in 60 mL CH2Cl2 at room temperature is added a solution of 10.0 g of trimethylsulfonium methylsulfate in 15 mL H2O. The resulting solution is set stirring and cooled to 0° C. Aqueous NaOH (50% w/w; 40 mL) is added in portions while stirring and the mixture subsequently refluxed for 1 h. After cooling to room temperature, the mixture is filtered and the filtrate extracted with CH2Cl2. The combined extracts are dried over MgSO4, filtered, and concentrated to yield a red oil, which is subjected to Kugelrohr distillation under high vacuum at 150° C. to yield 838 mg of the title compound as a clear, light yellow oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06852731B2 |
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| Quelldatensatz | uspto-grants-2005_02 |
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| ORD ID | ord-80408188b07545bfbcf381ecf1bc3f7b |
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| Quellennotiz | uspto-grants-2005_02 |
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