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HRID 276164作成日:2026年10月26日

Benzaldehyde → Heptanophenone

https://huagongshe.com/reaction/276164

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1-HexeneHCID 11597—
反応物2-Amino-3-methylpyridineHCID 15347—
生成物HeptanophenoneHCID 74282—

反応手順

Under the same reaction procedure and conditions as in Example 1 (benzaldehyde 0.5 mmol, 2-amino-3-picoline 0.1 mmol, 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 0.01 mmol. While the reactor was stopped with a stopper, the reactants were stirred at 130 ° C. for various reaction times as shown in the following table 9. After completion of the reaction, gas chromatography was conducted to determine the yields of heptanophenone, products according to various period of times and the results are given in Table 9, 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-6d0b7f1629d24a4bbff19960937cbd29
出典メモuspto-grants-2002_03