Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Triethoxysilane | HCID 13830 | — |
| Edukt | 4-(Phenylacetyl)morpholine | HCID 236601 | — |
| Katalysator | Titanium isopropoxide | HCID 11026 | — |
| Lösungsmittel | Benzene | HCID 241 | — |
| Produkt | 4-(2-Phenylethenyl)morpholine | HCID 54492098 | 63,4% |
Reaktionsschritte
4-(2-phenylacetyl) morpholine (0.410 g, 2.0 mmol) was dissolved in C6H6 (5 mL) under a nitrogen atmosphere and then triethoxysilane (0.92 mL, 5.0 mmol) and titanium (IV) isopropoxide (0.03 mL, 0.1 mmol) were added. The reaction mixture was heated to 60° C. for 15 hours. The C6H6 was removed in vacuo and the resulting cream colored solid was dissolved in warm (60° C.) hexane (3 mL). The hexane solution was cooled to room temperature, and cream colored crystals appeared in the flask. The recrystallization flask was put in an acetone-filled dewar, which was cooled to -78° C. overnight. The hexane solution was decanted from the cream colored crystals which were dried in vacuo, and 0.38 g of product was collected, although 1H NMR showed the presence of a silicon byproduct. The material was dissolved in 3 mL of warm hexane (60 ° C.) and slowly cooled to room temperature. The hexane was decanted and the product was dried in vacuo to produce 0.24 g (63% yield) of 4-(2-phenylethenyl) morpholine as a cream colored solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05220020 |
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| Quelldatensatz | uspto-grants-1993_06 |
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| ORD ID | ord-381f38378652476bb1cfceb248d37327 |
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| Quellennotiz | uspto-grants-1993_06 |
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