Hydrochloric Acid → 2,2-difluoro-2',3'-dihydro-1'H-spiro[cyclopropane-1,4'-quinoline]
Reaktionsgleichung
[F:1][C:2]1([F:22])[C:4]2([C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[N:7](NC(OC(C)(C)C)=O)[CH2:6][CH2:5]2)[CH2:3]1.Cl>ClCCl.O1CCOCC1>[F:22][C:2]1([F:1])[C:4]2([C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[NH:7][CH2:6][CH2:5]2)[CH2:3]1Komponenten
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
0.105 g of tert-butyl 2,2-difluoro-2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-quinoline]-1′-carbamate is dissolved in 5 ml of dichloromethane and then 7.78 ml of a 4N solution of hydrochloric acid in dioxane are added. Stirring is maintained for 14 hours. After evaporating, the residue is taken up in dichloromethane and then hydrolyzed with a saturated solution of sodium hydrogencarbonate in water. The mixture is extracted twice with dichloromethane. The organic phases are combined, washed with water and then with a saturated solution of sodium hydrogencarbonate in water and then dried over magnesium sulfate and the solvent is evaporated under reduced pressure. 0.588 g of 2,2-difluoro-2′,3′-dihydro-1′H-spiro[cyclopropane-1,4′-quinoline] is obtained.
Aufarbeitung
- temperatureis maintained for 14 hours
- customAfter evaporating
- extractionThe mixture is extracted twice with dichloromethane
- washwashed with water
- dry with materialwith a saturated solution of sodium hydrogencarbonate in water and then dried over magnesium sulfate
- customthe solvent is evaporated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-dfa71f3a240040edae4abdcdfda9641e
- Quelldatensatz
- uspto-grants-2011_05
- Patentnummer
- US07947834B2
Notizen zur Reaktion
Wird geladen…