Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Edukt | Phosphorus oxychloride | HCID 24813 | — |
| Edukt | 2-bromo-N-(2-phenylethyl)benzamide | HCID 673840 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | 1-(2-Bromophenyl)-3,4-dihydroisoquinoline | HCID 10779537 | — |
Reaktionsschritte
A suspension of 50.0 g (164 mmol) of N-phenylethyl-2-bromobenzamide and 27.9 g of phosphorus pentoxide in 200 ml of xylene was heated to 100° C. and admixed dropwise with 45.6 g (492 mmol) of phosphorus oxychloride. Subsequently, the reaction mixture was heated under reflux for 2 h. After cooling to 80° C., the reaction mixture was stirred into 4000 g of ice and adjusted to pH=12 with NaOH (solid). The organic phase was removed, the aqueous phase was extracted three times with 300 ml of toluene, and the combined organic phases were washed with 500 ml of water and subsequently dried over magnesium sulfate. After the desiccant had been filtered off and the solvent had been removed, the product was obtained as a yellow oil. The yield at a purity of approx. 99.0% was 46.9 g (164 mmol), 99.9% of theory.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07820822B2 |
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| Quelldatensatz | uspto-grants-2010_10 |
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| ORD ID | ord-9b952819493b4769b5d1cf44d622c65b |
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| Quellennotiz | uspto-grants-2010_10 |
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