Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 967626Erstellt: 25. Oktober 2026

Methyl 4-Formylbenzoate → 4-[(4-Cyclohexylphenylimino)methyl]benzoic acid methyl ester

https://huagongshe.com/reaction/967626

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 4-FormylbenzoateHCID 15294—
Edukt4-CyclohexylbenzenamineHCID 80764—
LösungsmittelMethanolHCID 887—
Produkt4-[(4-Cyclohexylphenylimino)methyl]benzoic acid methyl esterHCID 6748332384,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4-Formylbenzoic acid methyl ester (6.65 g, 40.5 mmol) was dissolved in hot methanol (175 mL). To this mixture, 4-cyclohexylaniline (7.1 g, 40.5 mmol) was added. To the resulting suspension, more methanol (75 mL) was added and the mixture was heated at reflux for 1 hour. After cooling to 0° C., the mixture was filtered and the solid was washed with ice-cold methanol and dried in vacuo at 40° C. for 16 hours to afford 10.95 g of 4-[(4-cyclohexylphenylimino)-methyl]benzoic acid methyl ester. This compound (10.93 g, 34 mmol) was suspended in methanol (200 mL) and glacial acetate acid (27 mL) was added followed by sodium cyano borohydride (1.9 g, 30 mmol) in small portions. The mixture was stirred at room temperature for 1 hour and concentrated in vacuo. The residue was dissolved in DCM (200 mL) and washed with 5% aqueous sodium carbonate (5×80 mL), dried (magnesium sulphate) and concentrated in vacuo. The residue was added ethyl acetate (100 mL) and n-heptane (200 mL) and concentrated in vacuo to half the original volume. The solid was filtered, washed with n-heptane and dried in vacuo at 40° C. for 16 hours to afford 9.52 g (87%) of 4-((4-cyclohexylphenylamino)methyl)benzoic acid methyl ester.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06953812B2
Quelldatensatzuspto-grants-2005_10
ORD IDord-4d5ac7d71bc34307adc008c794aee543
Quellennotizuspto-grants-2005_10