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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 24377Erstellt: 23. Oktober 2026

Triphenylphosphine → 3,5-Diisopropyl-4-(2-morpholin-4-ylethoxy)-benzaldehyde

https://huagongshe.com/de/reaction/24377

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt2-MorpholinoethanolHCID 61163—
Edukt4-Hydroxy-3,5-bis(isopropyl)benzaldehydeHCID 82712—
EduktDiethyl azodicarboxylateHCID 5462977—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt3,5-Diisopropyl-4-(2-morpholin-4-ylethoxy)-benzaldehydeHCID 2257113014,4%

Reaktionsschritte

Triphenylphosphine (5.14 g, 19.58 mmol) was added to a solution of 3,5-diisopropyl-4-hydroxybenzaldehyde (4 g, 19.58 mmol) in tetrahydrofuran (40 ml) followed by addition of 2-hydroxyethylmorpholine (2.57 g, 19.58 mmol) and then the dropwise addition of diethylazodicarboxylate (3.41 g, 19.58 mmol). The mixture was stirred at room temperature for 12 hours. The reaction was concentrated under reduced pressure and partitioned between 2N hydrochloric acid (200 ml) and ethyl acetate (150 ml). The aqueous layer was extracted with ethyl acetate (2×150ml), basified to pH 9 with solid sodium bicarbonate and extracted with ethyl acetate (3×150 ml). The organic layers were combined, dried over magnesium sulfate and concentrated to afford 900 mg (14%) of 3,5-diisopropyl-4-(2-morpholin-4-ylethoxy)-benzaldehyde as a yellowish oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855730B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-0b39b6e87327452e9407713dc876b76e
Quellennotizuspto-grants-2005_02