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 | — |
| 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 various transition metal catalysts as shown in the following table 6 were added to 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 according to various transition metal catalysts. The results are shown in Table 6, below.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US06353139B1 |
|---|
| Quelldatensatz | uspto-grants-2002_03 |
|---|
| ORD ID | ord-0b2b3a60d24044dfbcbd6ee1f35c0342 |
|---|
| Quellennotiz | uspto-grants-2002_03 |
|---|