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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 276158생성일: 2026년 10월 25일

Benzaldehyde → 2-Aminopyridine

https://huagongshe.com/reaction/276158

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물Benzoic AcidHCID 243—
반응물TolueneHCID 1140—
반응물AnilineHCID 6115—
반응물2-AminopyridineHCID 10439—
반응물1-HexeneHCID 11597—
생성물2-AminopyridineHCID 10439—
생성물HeptanophenoneHCID 74282—

반응 조건

온도130 °C

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06353139B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-fcceb4075c5c400f8b93bb53365b92fa
출처 메모uspto-grants-2002_03