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HRID 276162作成日:2026年10月25日

Benzaldehyde → Phosphine

https://huagongshe.com/reaction/276162

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—
反応物PhosphineHCID 24404—
生成物PhosphineHCID 24404—
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 [Rh(C8H14)2Cl]2 0.01 mmol and various phosphine ligands 0.025 mmol as shown in the following table 7 were introduced into 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 from various phosphine ligands. The results are given in Table 7, 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-e7fd9fc248924b249dac1da98ef8d5c3
出典メモuspto-grants-2002_03