2-Bromoethanol → HCID 23367219, compound
Reaction equation
[CH3:1][C:2]1[S:6][CH:5]=[N:4][CH:3]=1.[O:7]1CCO[CH2:9][CH2:8]1.[Br:13]CCO>CC(C)=O>[Br-:13].[OH:7][CH2:8][CH2:9][N+:4]1[CH:3]=[C:2]([CH3:1])[S:6][CH:5]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To the mixture of 5-methylthiazole (10 g) and dioxane (20 ml) was added 2-bromoethanol (15 g), and the resulting mixture was heated under reflux for 4 hours. To the mixture left standing at room temperature for about 0.5 hour was added acetone (100 ml) with stirring to crystallize pale yellow solids. The supernatant was discarded, and acetone (50 ml) and ether (150 ml) were added with stirring to give white to pale yellow solids, which were collected by filtration, washed with ether and dried under reduced pressure.
Workup
- temperaturethe resulting mixture was heated
- temperatureunder reflux for 4 hours
- waitTo the mixture left
- customto crystallize pale yellow solids
- additionacetone (50 ml) and ether (150 ml) were added
- stirringwith stirring
- customto give white to pale yellow solids, which
- filtrationwere collected by filtration
- washwashed with ether
- customdried under reduced pressure
Sources & evidence
- ORD record
- ord-7bcc7018bf434a459f60332cfd421457
- Source dataset
- uspto-grants-1996_12
- Patent number
- US05580904
Reaction notes
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