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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 11209Erstellt: 24. Oktober 2026

Diethyl Ether → (2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol

https://huagongshe.com/de/reaction/11209

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktSodium HydroxideHCID 14798—
EduktBupropion Morpholinol (2R,3R)-IsomerHCID 9943907—
LösungsmittelWaterHCID 962—
Produkt(2R,3R)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinolHCID 9943908—

Reaktionsschritte

(+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride may be converted back to its free base by the following process. A 3.0 g sample of (+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol hydrochloride was dissolved in water (100 mL) and diethyl ether was added (200 mL). The mixture was chilled in an ice bath and the pH was adjusted to >10 with 1.0N aqueous sodium hydroxide. After stirring for 30 min., the phases were separated and the aqueous phase was extracted with diethyl ether. The combined diethyl ether extracts were dried (Na2SO4) and concentrated in vacuo to give 2.6 g of (+/−)-(2R*,3R*)-2-(3-chlorophenyl)-3,5,5-trimethyl-2-morpholinol as a white solid. This was used without further purification for the chiral chromatography described below.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07098206B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-ccf1d5796b1247748d63c86e697ede67
Quellennotizuspto-grants-2006_08