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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276162Erstellt: 24. Oktober 2026

Benzaldehyde → Phosphine

https://huagongshe.com/de/reaction/276162

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktBenzoic AcidHCID 243—
EduktTolueneHCID 1140—
EduktAnilineHCID 6115—
Edukt1-HexeneHCID 11597—
Edukt2-Amino-3-methylpyridineHCID 15347—
EduktPhosphineHCID 24404—
ProduktPhosphineHCID 24404—
ProduktHeptanophenoneHCID 74282—

Reaktionsbedingungen

Temperatur130 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353139B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-e7fd9fc248924b249dac1da98ef8d5c3
Quellennotizuspto-grants-2002_03