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 0.1mmol, 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 1 0.01 mmol. While the reactor was stopped with a stopper, the reactants were stirred at various temperatures (70-130° C.) as shown in the following table 10 for 1 hour. After completion of the reaction, gas chromatography was conducted to determine the yields of heptanophenone, products according to various temperatures and the results are given in Table 10, below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06353139B1 |
| Source dataset | uspto-grants-2002_03 |
| ORD ID | ord-513cbb7ec128432190a40b608fe0b8bb |
| Source note | uspto-grants-2002_03 |