Reaktionsgleichung
[NH2:1][C:2]1[CH:7]=[C:6]([NH2:8])[CH:5]=[CH:4][C:3]=1[CH3:9].N[C:11](N)=[O:12].[C:14](=[O:19])([O:16][CH2:17][CH3:18])N.[CH2:20]([OH:22])[CH3:21]>>[CH2:17]([O:16][C:14]([NH:1][C:2]1[CH:7]=[C:6]([NH:8][C:11]([O:22][CH2:20][CH3:21])=[O:12])[CH:5]=[CH:4][C:3]=1[CH3:9])=[O:19])[CH3:18]Komponenten
5
Versuchsvorschrift
Following the procedure described in Example 1, 611 g of 2,4-diaminotoluene, 480 g of urea, 178 g of ethyl carbamate and 1590 g of ethanol (approximately 96%) were reacted for 6.5 hours at 200° C. in the pressure apparatus described in Example 1. After cooling and venting of the apparatus, the reaction mixture was removed, filtered and analyzed by liquid chromatography (HPLC). A yield of 881 g (66% of the theoretical yield) of 2,4-bis-(ethoxy carbonyl amino)-toluene was determined.
Aufarbeitung
- customwere reacted for 6.5 hours at 200° C. in the pressure apparatus
- temperatureAfter cooling
- customthe reaction mixture was removed
- filtrationfiltered
Quellen und Nachweise
- ORD-Eintrag
- ord-3bf43103a77049c2bfe8cd027a42ed61
- Quelldatensatz
- uspto-grants-1984_02
- Patentnummer
- US04430505
Verknüpfte Notizen
Wird geladen…