Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Edukt | Formamide, N-(2-phenylethyl)- | HCID 140995 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 3,4-Dihydroisoquinoline | HCID 76705 | — |
Reaktionsschritte
A 250 mL round bottom flask equipped with stir bar, reflux condenser, and an addition funnel is charged with phosphorus pentoxide (7.07 g) and polyphosphoric acid in a 10.5:1 weight ratio. The mixture is stirred and heated at approximately 180° C. for about 1 hour, then cooled to approximately 150° C. The cooled, crude phenethylformamide prepared as described above is added dropwise to this mixture. On complete addition the reaction is heated and stirred at approximately 170° C. overnight. The mixture is cooled to room temperature and diluted with water (300 mL), washed with diethyl ether (150 mL) and cooled in an acetone/dry ice bath while the pH is adjusted to 9 with saturated potassium hydroxide. The aqueous solution is extracted with ether (3×150 mL) and the pooled organics are dried over magnesium sulfate, filtered, and concentrated under reduced pressure to yield an oil that is further purified via Kugelrohr distillation (70° C., 1 mm Hg) to give the compound of formula 2.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05817614 |
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| Quelldatensatz | uspto-grants-1998_10 |
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| ORD ID | ord-af0bf58df29f4d24baf33cff16d27aac |
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| Quellennotiz | uspto-grants-1998_10 |
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