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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 128912Erstellt: 25. Oktober 2026

1-Phenyl-1-propanol → alpha-(1-imidazolyl)-2-(1-phenylpropyloxy)benzaldehyde O-methyloxime

https://huagongshe.com/reaction/128912

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Phenyl-1-propanolHCID 7147—
EduktTriphenylphosphineHCID 11776—
Eduktethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Edukt2-hydroxy-alpha-(1-imidazolyl)benzaldehyde O-methyloximeHCID 135976165—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelTetrahydrofuranHCID 8028—
Produktalpha-(1-imidazolyl)-2-(1-phenylpropyloxy)benzaldehyde O-methyloximeHCID 5451549394,9%

Reaktionsschritte

Triphenylphosphine (1.05 g), 1-phenylpropyl alcohol (0.54 g) and THF (20 ml) were added to 2-hydroxy-α-(1-imidazolyl)benzaldehyde O-methyloxime (0.43 g), and diethyl azodicarboxylate (0.70 g) was added under ice-cooling over 10 minutes. Then the mixture was stirred at room temperature for 2 hours. After completion of the reaction, ether (100 ml) was added, the mixture was washed with water (80 ml) twice, and the ether layer was concentrated under reduced pressure. The resulting crude product was purified by silica gel chromatography to give α-(1-imidazolyl)-2-(1-phenylpropyloxy)benzaldehyde O-methyloxime (0.63 g) as a colorless oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05466661
Quelldatensatzuspto-grants-1995_11
ORD IDord-4d2ce26ab71a473abd85b8cc9ab46a21
Quellennotizuspto-grants-1995_11