Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl formate | HCID 8025 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | ethyl 2-((tetrahydro-2H-pyran-2-yl)oxy)acetate | HCID 10899396 | — |
| Edukt | Cinnamimidamide | HCID 14668188 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Tetrahydrofuran | HCID 8028 | — |
| Lösungsmittel | Ethanol, mixt. with methanol | HCID 18681192 | — |
| Produkt | HCID 178517727 | HCID 178517727 | 63,2% |
Reaktionsschritte
NaH (0.38 g, 9.5 mmol, 60% paraffin oil) was added slowly to a THF (20 mL) solution of ethyl (tetrahydro-2H-pyran-2-yloxy)acetate (prepared by treating ethyl hydroxyacetate with 3,4-dihydro-2H-pyran and TsOH) (1.0 g, 5.3 mmol) and dry ethyl formate (3.9 g, 53 mmol). The reaction mixture was stirred at room temperature for 15 min. and then heated at 65° C. for 45 min. The reaction mixture was concentrated to dryness to give a pale yellow solid. The solid was added to a MeOH/EtOH (20 mL/20 mL) solution of (2E)-3-phenyl-2-propenimidamide (0.78 g, 5.3 mmol), the subsequent mixture was heated at 80° C. for 4 h. The resulting material was poured into DCM (10 mL) containing silica gel (3 g) and evaporated. Purification by column chromatography (silica gel) using a MeOH/DCM gradient (0-10%) provided the desired product as a pale yellow solid (1 g, 63%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08071592B2 |
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| Quelldatensatz | uspto-grants-2011_12 |
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| ORD ID | ord-6879b79ccf234b85af1804df33b3675c |
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| Quellennotiz | uspto-grants-2011_12 |
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