Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Benzaldehyde | HCID 240 | — |
| Edukt | Benzoic Acid | HCID 243 | — |
| Edukt | Toluene | HCID 1140 | — |
| Edukt | Aniline | HCID 6115 | — |
| Edukt | 1-Hexene | HCID 11597 | — |
| Edukt | 2-Amino-3-methylpyridine | HCID 15347 | — |
| Edukt | Phosphine | HCID 24404 | — |
| Produkt | Phosphine | HCID 24404 | — |
| 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, aniline 0.3 mmol, bezoic acid 0.03 mmol, 1-hexene 2.5 mmol, toluene 0.87 mmol), the mixture in a 500 ml pressure reactor was stirred at normal temperature for 2-3 minutes and then [Rh(C8H14)2Cl]2 0.01 mmol and various phosphine ligands 0.025 mmol as shown in the following table 7 were introduced into each reactor. 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, gas chromatography was conducted to determine the yields of heptanophenone, products from various phosphine ligands. The results are given in Table 7, 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-e7fd9fc248924b249dac1da98ef8d5c3 |
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| Quellennotiz | uspto-grants-2002_03 |
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