Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Propionate | HCID 7749 | — |
| Edukt | 4-Pyridinecarboxaldehyde | HCID 13389 | — |
| Edukt | Sodium Methoxide | HCID 10942334 | — |
| Edukt | 4,5,6,7-Tetrahydro-2-benzofuran-1(3H)-one | HCID 12579014 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Produkt | HCID 178514951 | HCID 178514951 | — |
Reaktionsschritte
Four portions each of 0.99 ml 5.4 M methanolic sodium methylate solution (21.4 mmol) are stirred into a solution of 2.957 g (21.4 mmol) 4,5,6,7-tetrahydro-1(3H)-isobenzofuranone (for preparation see J. Am. Chem. Soc. 118, 1-12 [1996]), 2.02 ml (21.4 mmol) pyridine-4-carbaldehyde, and 10.7 ml (93.2 mmol) ethyl propionate in 17.4 ml methanol at intervals of 5 min respectively and at 0° C. The reaction mixture is stirred for 20 min at RT, heated for 2 h under reflux, and then evaporated under vacuum. Stirring of the residue in 5 ml water, filtration, washing of the filter residue with water, and drying under HV (8 h, 100° C.) yields the title compound; m.p. 258-261° C.; ESI-MS: (M+H)+=228. A further, slightly impure batch of title compound may be obtained by extracting the aqueous filtrate with diethylether, adjusting the aqueous phase to pH 7 with glacial acetic acid, filtering, and washing the filter residue with water.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06710047B2 |
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| Quelldatensatz | uspto-grants-2004_03 |
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| ORD ID | ord-a04317dc604c4abf975d9a0e8fe5f4e4 |
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| Quellennotiz | uspto-grants-2004_03 |
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