Hydrogen Bromide → HCID 54540372, compound
Reaction equation
[C:1]1([CH:11]2[C:16](=[O:17])[NH:15][C:14](=[O:18])[NH:13][C:12]2=[O:19])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][CH:2]=1.[BrH:20].BrBr>C(O)C>[Br:20][C:11]1([C:1]2[C:10]3[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=3)[CH:4]=[CH:3][CH:2]=2)[C:16](=[O:17])[NH:15][C:14](=[O:18])[NH:13][C:12]1=[O:19]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
A suspension of 5-naphtylbarbituric acid (0.2 g) in 1.5 ml of 95% ethanol, cooled at 0° C. and kept under stirring, is added dropwise with 48% hydrobromic acid (0.5 ml) and successively with 4.4 μl of bromine. After 4 hours under stirring at room temperature the solid is filtered and washed with water, then it is dried under vacuum at 40° C. overnight. 0.25 g of the product are obtained.
Workup
- stirringAfter 4 hours under stirring at room temperature the solid
- filtrationis filtered
- washwashed with water
- customit is dried under vacuum at 40° C. overnight
Sources & evidence
- ORD record
- ord-7befe694130c42abb1792811d2a848c0
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06110924
Reaction notes
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