HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → Heptanophenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Benzoic Acid | HCID 243 | — |
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Aniline | HCID 6115 | — |
| Reactant | 1-Hexene | HCID 11597 | — |
| Reactant | 2-Amino-3-methylpyridine | HCID 15347 | — |
| Product | Heptanophenone | HCID 74282 | — |
Reaction Steps
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 combined with Rh(PPh3)3Cl 0.01 mmol. While the reactor was stopped with a stopper, the reactants were stirred at 130 ° C. for various reaction times as shown in the following table 9. After completion of the reaction, gas chromatography was conducted to determine the yields of heptanophenone, products according to various period of times and the results are given in Table 9, below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353139B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-6d0b7f1629d24a4bbff19960937cbd29 |
| Source note | uspto-grants-2002_03 |