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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 654322Erstellt: 25. Oktober 2026

Atenolol → Atenolol p-toluate

https://huagongshe.com/reaction/654322

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAtenololHCID 2249—
EduktP-Toluic AcidHCID 7470—
LösungsmittelAcetoneHCID 180—
ProduktAtenolol p-toluateHCID 86745986—

Reaktionsschritte

The atenolol having low optical purity (1 mole) and p-toluic acid (1 mole) are dissolved in acetone (5 to 50 liters) with heating and the mixture is stirred at 0° to 15° C. for 5 to 24 hours. The precipitated crystals are removed by filtration, and the mother liquor is concentrated to give an optically active atenolol p-toluate with having higher optical purity, for example a salt having an optical purity of 98% ee or more from a salt having an optical purity of 91% ee in a yield of 50to 80%. In this method, when benzoic acid is used instead of p-toluic acid and chloroform is used instead of acetone, similar result is obtained. When p-t-butylbenzoic acid is used instead of p-toluic acid in the above method, the produced salt is hardly soluble in a solvent, and hence, it is necessary to use a solvent having higher solubility such as ethanol or 2-propanol instead of acetone.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05130482
Quelldatensatzuspto-grants-1992_07
ORD IDord-689485422967476a86cb81a82ba04ac4
Quellennotizuspto-grants-1992_07