Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sulfuric Acid | HCID 1118 | — |
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Diisobutylaluminum hydride | HCID 14487 | — |
| Edukt | 6-Chloro-3-pyridinecarbonitrile | HCID 5152094 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | 6-Chloropyridine-3-carbaldehyde | HCID 2764053 | 62% |
Reaktionsschritte
Combine 6-chloro-nicotino-nitrile (1.00 g, 7.21 mmol) and toluene (24 mL). Cool the resulting solution at 0° C. and add DIBAL-H (1.0 M in toluene, 7.58 mL, 7.58 mmol) dropwise. Stir the resulting red solution at 0° C. for 1 h. Then, add methanol (2 mL) followed by H2SO4 (aq. 2.0 M, 6 mL). Stir for 1 h at rt. Add CHCl3:isopropanol (3/1, 15 mL) and wash with Rochelle's salt solution (20 mL), followed by NaHCO3 (20 mL) and brine. Dry the combined organic layers over magnesium sulfate, filter and concentrate. Purify by flash chromatography (EtOAc/hexanes 10%) to give the title compound (530 mg, 62%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07381719B2 |
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| Quelldatensatz | uspto-grants-2008_06 |
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| ORD ID | ord-11f65d50ccb94616be56241ee9ec4429 |
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| Quellennotiz | uspto-grants-2008_06 |
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