Formic Acid → N-(4-hydroxy-2,3,6-trimethylphenyl)formamide
Reaktionsgleichung
[NH2:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([OH:9])=[C:4]([CH3:10])[C:3]=1[CH3:11].[CH:12](O)=[O:13]>>[CH:12]([NH:1][C:2]1[C:7]([CH3:8])=[CH:6][C:5]([OH:9])=[C:4]([CH3:10])[C:3]=1[CH3:11])=[O:13]Komponenten
3
Versuchsvorschrift
4-Amino-2,3,5-trimethylphenol (100 g, 662 mmol) was dissolved in formic acid (500 ml). The mixture was heated under reflux for 36 hours. The reaction mixture was poured into ice-cold water. The precipitated crystals were filtered, washed with water and dried. The crude crystals obtained were recrystallized from ethanol to obtain the desired compound (85.9 g, yield: 72.5%), m.p. 219°-220° C.
Aufarbeitung
- temperatureThe mixture was heated
- temperatureunder reflux for 36 hours
- additionThe reaction mixture was poured into ice-cold water
- filtrationThe precipitated crystals were filtered
- washwashed with water
- customdried
- customThe crude crystals obtained
- customwere recrystallized from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-113cd4d0a87a464e9ef309e8080f4b39
- Quelldatensatz
- uspto-grants-1997_01
- Patentnummer
- US05594154
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