참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzaldehyde | HCID 240 | — |
| 반응물 | Benzoic Acid | HCID 243 | — |
| 반응물 | Toluene | HCID 1140 | — |
| 반응물 | Aniline | HCID 6115 | — |
| 반응물 | 2-Aminopyridine | HCID 10439 | — |
| 반응물 | 1-Hexene | HCID 11597 | — |
| 생성물 | 2-Aminopyridine | HCID 10439 | — |
| 생성물 | Heptanophenone | HCID 74282 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06353139B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-fcceb4075c5c400f8b93bb53365b92fa |
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| 출처 메모 | uspto-grants-2002_03 |
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