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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 236568Erstellt: 24. Oktober 2026

Potassium Carbonate → alpha-Ethyl-alpha-(4-chlorophenyl)-4-[3-(di-n-propylamino)-propoxy]-benzylalcohol

https://huagongshe.com/de/reaction/236568

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktDipropylaminopropyl chlorideHCID 12333917—
Eduktalpha-Ethyl-alpha-(4-chlorophenyl)-4-hydroxy-benzylalcoholHCID 14727318—
KatalysatorTetrabutylammonium hydrogen sulfateHCID 94433—
LösungsmittelEthyl AcetateHCID 8857—
Produktalpha-Ethyl-alpha-(4-chlorophenyl)-4-[3-(di-n-propylamino)-propoxy]-benzylalcoholHCID 20216260—

Reaktionsschritte

13.1 g. of α-ethyl-α-(4-chlorophenyl)-4-hydroxy-benzylalcohol, 14 g. of anhydrous potassium carbonate, 9.8 g. of dipropylaminopropyl chloride and 0.85 g. of tetrabutyl ammonium hydrogensulfate in 135 ml. of ethyl acetate are slightly boiled for 20 hours, under stirring. After cooling the mixture, the solvent is evaporated in vacuo. To the residue water and benzene are added. The phases are separated, the benzene solution is washed with water, dried over anhydrous potassium carbonate, filtered and evaporated. The residue is purified by vacuum fractionation. 13.8 g. of the desired end product are obtained, boiling at 198° to 200° C./1.33 Pa.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04645779
Quelldatensatzuspto-grants-1987_02
ORD IDord-207e32b5a3714d40af02fe0ad4959c98
Quellennotizuspto-grants-1987_02