関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Benzaldehyde | HCID 240 | — |
| 反応物 | Benzoic Acid | HCID 243 | — |
| 反応物 | Toluene | HCID 1140 | — |
| 反応物 | Aniline | HCID 6115 | — |
| 反応物 | 2-Aminopyridine | HCID 10439 | — |
| 反応物 | 1-Hexene | HCID 11597 | — |
| 生成物 | 2-Aminopyridine | HCID 10439 | — |
| 生成物 | Heptanophenone | HCID 74282 | — |
反応手順
Under the same reaction procedure and conditions as in Example 1 (benzaldehyde 0.5 mmol, aniline 0.3 mmol, bezoic acid 0.03 mmol, 1-hexene 2.5 mmol, toluene 0.87 mmol), various 2-aminopyridine derivatives 0.1 mmol as shown in the following table 3, 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, gas chromatography was conducted to determine the yields of heptanophenone, products from various aminopyridine derivatives. The results are presented in Table 3, below.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US06353139B1 |
|---|
| 出典データセット | uspto-grants-2002_03 |
|---|
| ORD ID | ord-fcceb4075c5c400f8b93bb53365b92fa |
|---|
| 出典メモ | uspto-grants-2002_03 |
|---|