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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 647148Erstellt: 24. Oktober 2026

Hydrochloric Acid → 3'-(Benzyloxy)-2-isopropylamino-acetophenone hydrochloride

https://huagongshe.com/de/reaction/647148

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
EduktIsopropylamineHCID 6363—
Edukt1-(3-(Benzyloxy)phenyl)-2-bromoethanoneHCID 88031—
LösungsmittelEthanolHCID 702—
Produkt3'-(Benzyloxy)-2-isopropylamino-acetophenone hydrochlorideHCID 20134461—

Reaktionsschritte

In 425 ml of ethanol, 64 g of 3-benzyloxyphenacyl bromide and 212 ml of iso-propylamine are stirred at 5° C. under N2 atmosphere, and the temperature is allowed to rise to 12° C. After 0.75 minutes, the clear solution is poured into 2 liters of crushed ice containing 500 ml of concentrated HCl and 1.5 liters of H2O. The mixture is stirred for 20 minutes, filtered and the solid is washed with water to afford 3'-(benzyloxy)-2-isopropylamino-acetophenone hydrochloride, mp 213°-215° C. dec.. A 5 g-sample of this material is stirred in 50 ml of methanol, and the mixture is cooled in ice and neutralized with 10% NaOH until a clear solution is obtained. To this solution, 2 g of NaBH4 is added and after 0.75 hours of stirring, the mixture is evaporated in vacuo, and the resulting solid is collected and washed with H2O. This gives, after drying, 4.4 g of m-(benzyloxy)-α-[(isopropylamino)methyl]benzyl alcohol, mp 83°-85° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04407819
Quelldatensatzuspto-grants-1983_10
ORD IDord-d06a27a74e514d67a12d24ed9c4c6676
Quellennotizuspto-grants-1983_10