Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyrrolidine | HCID 31268 | — |
| Edukt | 2-Fluoro-5-formylpyridine | HCID 16414246 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Produkt | 6-(Pyrrolidin-1-yl)pyridine-3-carbaldehyde | HCID 2794775 | 84,5% |
Reaktionsschritte
6-Fluoro-3-pyridinecarboxaldehyde (152 mg, 1.22=01) was dissolved in tetrahydrofuran (3.0 mL). To this, pyrrolidine (507 μL, 6.08 mmol) was added under a nitrogen atmosphere at room temperature and the mixture was stirred at the same temperature for 2 hours and successively at 60° C. for 5 hours. The reaction mixture was concentrated, and the residue was purified by silica gel column chromatography (hexane/ethyl acetate=1/1) to give 6-(pyrrolidin-1-yl)-3-pyridinecarboxaldehyde (181 mg, yield: 84%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08673908B2 |
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| Quelldatensatz | uspto-grants-2014_03 |
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| ORD ID | ord-2e99f33994db471c9e54fae6db85b2d4 |
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| Quellennotiz | uspto-grants-2014_03 |
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