Thiazole → 3-(2-Hydroxyethyl)-1,3-thiazol-3-ium bromide
Reaktionsgleichung
[S:1]1[CH:5]=[CH:4][N:3]=[CH:2]1.[Br:6][CH2:7][CH2:8][OH:9]>>[Br-:6].[OH:9][CH2:8][CH2:7][N+:3]1[CH:4]=[CH:5][S:1][CH:2]=1Komponenten
3
Versuchsvorschrift
Thiazole (4.3 g) and 2-bromoethanol (12.5 g) were mixed and heated under reflux for 5 hours. The reaction was left standing at room temperature to give white needles. The crystals were washed with acetone, collected by filtration and dried under reduced pressure.
Aufarbeitung
- temperatureheated
- temperatureunder reflux for 5 hours
- waitThe reaction was left
- customstanding at room temperature
- customto give white needles
- washThe crystals were washed with acetone
- filtrationcollected by filtration
- customdried under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-6d8ff83a71c74d93878a9c194cdb7a9b
- Quelldatensatz
- uspto-grants-1996_12
- Patentnummer
- US05580904
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