戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 276158作成日:2026年10月26日

Benzaldehyde → 2-Aminopyridine

https://huagongshe.com/reaction/276158

反応式

関与物質

役割名称HCID仕込み量
反応物BenzaldehydeHCID 240—
反応物Benzoic AcidHCID 243—
反応物TolueneHCID 1140—
反応物AnilineHCID 6115—
反応物2-AminopyridineHCID 10439—
反応物1-HexeneHCID 11597—
生成物2-AminopyridineHCID 10439—
生成物HeptanophenoneHCID 74282—

反応条件

温度130 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06353139B1
出典データセットuspto-grants-2002_03
ORD IDord-fcceb4075c5c400f8b93bb53365b92fa
出典メモuspto-grants-2002_03