Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | Benzoic Acid | HCID 243 | — |
| Edukt | Toluene | HCID 1140 | — |
| Edukt | 1-Hexene | HCID 11597 | — |
| Edukt | 2-Amino-3-methylpyridine | HCID 15347 | — |
| Produkt | Heptanophenone | HCID 74282 | — |
Reaktionsschritte
Under the same reaction procedure and conditions as in Example 1 (benzaldehyde 0.5 mmol, 2-amino-3-picoline 0.1 mmol, bezoic acid 0.03 mmol, 1-hexene 2.5 mmol, toluene 0.87 mmol), various kinds of amines 0.3 mmol as shown in the following table 5, were added to each 500 ml pressure reactor. The mixture was stirred at normal temperature for 2-3 minutes and then combined with Rh(PPh3)3Cl 0.01 mmol. While the reactor was stopped with a stopper, the reactants were heated at 130° C. for 1 hour with stirring. After completion of the reaction, column chromatography was conducted to determine the yields of heptanophenone, products according to various amines. The results are given in Table 5, below.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06353139B1 |
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| Quelldatensatz | uspto-grants-2002_03 |
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| ORD ID | ord-e5e44ed7f59d431392a6aa614d158671 |
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| Quellennotiz | uspto-grants-2002_03 |
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