Acetic Anhydride → 5-Acetoxymethyl-2-phenyl-1H-imidazole
Reaktionsgleichung
[OH:1][CH2:2][C:3]1[NH:7][C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)=[N:5][CH:4]=1.[C:14](OC(=O)C)(=[O:16])[CH3:15]>C1(C)C=CC=CC=1>[C:14]([O:1][CH2:2][C:3]1[NH:7][C:6]([C:8]2[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=2)=[N:5][CH:4]=1)(=[O:16])[CH3:15]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 52.5 °C
Versuchsvorschrift
Mix 5-hydroxymethyl-2-phenyl-1H-imidazole (1.3 Kg) and toluene (10.4 L) at 20-25° C., and then heat the mixture with stirring to 50-55° C. Add acetic anhydride (780 ml, 1.1 equivalents) slowly and continue heating at 50-55° C. until the reaction is complete (typically 3-4 hours). Cool the reaction mixture to -5-0° C., filter off the product, wash it with toluene (3×700 ml) and then dry it under vacuum at 50-55° C. to constant weight.
Aufarbeitung
- temperatureheat the mixture
- customtypically 3-4 hours
- temperatureCool the reaction mixture to -5-0° C.
- filtrationfilter off the product
- washwash it with toluene (3×700 ml)
- customdry it under vacuum at 50-55° C. to constant weight
Quellen und Nachweise
- ORD-Eintrag
- ord-d1071a8770eb4aa4a263369ae4bc67cc
- Quelldatensatz
- uspto-grants-1999_05
- Patentnummer
- US05905152
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