Reaktionsgleichung
[OH:1][NH:2][C:3]([NH2:5])=[O:4].CO.CO[CH:10](OC)[CH2:11][C:12](=O)[CH2:13][CH3:14].C(O)C.[ClH:21]>>[ClH:21].[CH2:13]([C:12]1[N:5]=[C:3]([OH:4])[N+:2]([O-:1])=[CH:10][CH:11]=1)[CH3:14]Komponenten
Reaktionsbedingungen
- Temperatur
- -6.5 °C
Versuchsvorschrift
0.388 mol (25.9 g) hydroxy urea were dissolved in 195 ml 2 M HCl, 80 ml of methanol were added and 0.388 mol (56.7 g) of 1,1-dimethoxypentane-3-on (62% content in product mixture) were added dropwise under cooling with the internal temperature being maintained at −6 to −7° C. The solution was thawed to room temperature in an ice bath and stirred for 1 h, then evaporated until dryness. The residue was suspended with 100 ml of acetone, the mixture was cooled to below 0° C. in an ice/ethanol bath, the solid filtered off and washed with little ice-cold acetone. After drying 32.6 g crude product were obtained. The crude product was heated until boiling with 200 ml ethanol, hot filtered and slowly cooled to −18° C. The precipitated solid was filtered off, washed with a little amount of ethanol and dried. 11.7 g of the title compound were obtained.
Aufarbeitung
- temperatureunder cooling with the internal temperature
- customThe solution was thawed to room temperature in an ice bath
- customevaporated until dryness
- temperaturethe mixture was cooled to below 0° C. in an ice/ethanol bath
- filtrationthe solid filtered off
- washwashed with little ice-cold acetone
- dry with materialAfter drying 32.6 g crude product
- customwere obtained
- filtrationhot filtered
- temperatureslowly cooled to −18° C
- filtrationThe precipitated solid was filtered off
- washwashed with a little amount of ethanol
- customdried
Quellen und Nachweise
- ORD-Eintrag
- ord-dcb726fdc3bb4008bcf77046605c0b12
- Quelldatensatz
- uspto-grants-2016_08
- Patentnummer
- US09422247B2
Verknüpfte Notizen
Wird geladen…