Reaktionsgleichung
[F:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([F:14])[C:12]=1[F:13])[CH2:5][NH:6]CCO.[C:15]([O:22][CH2:23][CH3:24])(=[O:21])[C:16]([O:18]CC)=O>>[F:1][C:2]1[CH:3]=[C:4]([CH:10]=[C:11]([F:14])[C:12]=1[F:13])[CH2:5][N:6]1[CH2:24][CH2:23][O:22][C:15](=[O:21])[C:16]1=[O:18]Komponenten
3
Reaktionsbedingungen
- Temperatur
- 170 °C
Versuchsvorschrift
A mixture of 2-[(3,4,5-trifluorobenzyl)amino]ethanol (6.91 g) and diethyl oxalate (20 mL) was stirred at 170° C. for one hour. The reaction solution was concentrated under reduced pressure, and then a diethyl ether was added to the residue. The precipitated crystals were collected by filtration and then air-dried to obtain 7.38 g of the title compound.
Aufarbeitung
- concentrationThe reaction solution was concentrated under reduced pressure
- additiona diethyl ether was added to the residue
- filtrationThe precipitated crystals were collected by filtration
- customair-dried
Quellen und Nachweise
- ORD-Eintrag
- ord-94e074c546c94546a00db6bf96662b77
- Quelldatensatz
- uspto-grants-2009_11
- Patentnummer
- US07618960B2
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