Reaktionsgleichung
[C:1]([C:3]1[CH:4]=[C:5]([CH:9]2OCC[O:10]2)[CH:6]=[CH:7][CH:8]=1)#[CH:2].Cl>O>[C:1]([C:3]1[CH:4]=[C:5]([CH:6]=[CH:7][CH:8]=1)[CH:9]=[O:10])#[CH:2]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
A multinecked, round bottom flask fitted with a mechanical stirrer, reflux condenser and thermometer, was charged 50.4 g (0.289 mol) of the product of Example XI, 400 ml of distilled water and 1 of concentrated hydrochloric acid. The mixture was heated to 60° C. and maintained at that temperature for about 4 hours and then cooled to room temperature which yielded the product as a yellow precipitate. The product was filtered, washed with distilled water and allowed to dry on the funnel overnight to yield 33 g (0.254 mol, 87.8% yield).
Aufarbeitung
- customA multinecked, round bottom flask fitted with a mechanical stirrer
- temperaturereflux condenser
- temperaturemaintained at that temperature for about 4 hours
- temperaturecooled to room temperature which
- customyielded the product as a yellow precipitate
- filtrationThe product was filtered
- washwashed with distilled water
- customto dry on the funnel overnight
- customto yield 33 g (0.254 mol, 87.8% yield)
Quellen und Nachweise
- ORD-Eintrag
- ord-8bb514bf8c154fdfa0eb2fbb63fcb7f5
- Quelldatensatz
- uspto-grants-1988_08
- Patentnummer
- US04766251
Verknüpfte Notizen
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