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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276161Erstellt: 24. Oktober 2026

Benzaldehyde → Heptanophenone

https://huagongshe.com/de/reaction/276161

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzaldehydeHCID 240—
EduktBenzoic AcidHCID 243—
EduktTolueneHCID 1140—
EduktAnilineHCID 6115—
Edukt1-HexeneHCID 11597—
Edukt2-Amino-3-methylpyridineHCID 15347—
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 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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353139B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-0b2b3a60d24044dfbcbd6ee1f35c0342
Quellennotizuspto-grants-2002_03