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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 543580Erstellt: 25. Oktober 2026

Chloroform → 1-(1,2-Oxazolidin-2-yl)-2-{4-[4-(trifluoromethyl)phenoxy]phenoxy}propan-1-one

https://huagongshe.com/reaction/543580

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroformHCID 6212—
EduktTriethylamineHCID 8471—
EduktIsoxazolidine hydrochlorideHCID 12304500—
Edukt2-{4-[4-(Trifluoromethyl)phenoxy]phenoxy}propanoyl chlorideHCID 12906015—
LösungsmittelWaterHCID 962—
Produkt1-(1,2-Oxazolidin-2-yl)-2-{4-[4-(trifluoromethyl)phenoxy]phenoxy}propan-1-oneHCID 1327943697,7%

Reaktionsschritte

To a mixture of isoxazolidine hydrochloride (11.0 g) and chloroform (200 ml), under stirring and ice-cooling, was added (±)-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionyl chloride (34.5 g) and then added dropwise triethylamine (22.2 g). After the completion of addition, the reaction mixture was stirred for further 30 minutes at room temperature, to which water was added to form two layers. The organic layer so separated was washed with 1 N hydrochloric acid and then with 1 N aqueous sodium hydroxide and dried over anhydrous sodium sulfate. Removal of the solvent by a distillation in vacuo gave N-[(±)-2-[4-(4-trifluoromethylphenoxy)phenoxy]propionyl]isoxazolidine (37.3 g) as a white crystalline solid. After recrystallization from a mixture of n-hexane/acetone, the resulting white crystalline solid showed the melting point of 105°-107° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04447259
Quelldatensatzuspto-grants-1984_05
ORD IDord-a8959e1479f54b079121103f4d2ac70f
Quellennotizuspto-grants-1984_05