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HRID 276161作成日:2026年10月25日

Benzaldehyde → Heptanophenone

https://huagongshe.com/reaction/276161

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, 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 various transition metal catalysts as shown in the following table 6 were added to each reactor. 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 according to various transition metal catalysts. The results are shown in Table 6, 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-0b2b3a60d24044dfbcbd6ee1f35c0342
出典メモuspto-grants-2002_03