Hydrogen Bromide → HCID 18408835, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[C:14](=[O:15])[NH:13][C:12](=[O:16])[NH:11][C:10]2=[O:17])=[CH:5][CH:4]=1.[BrH:18].BrBr>O>[Br:18][C:9]1([C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=2)[C:10](=[O:17])[NH:11][C:12](=[O:16])[NH:13][C:14]1=[O:15]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 2.5 °C
Procedure
To a suspension of 5-(4-Methoxyphenyl)barbituric acid (222 mg) in 3 ml of water, cooled to 0-5° C. with ice bath, are added 136 μl of 48% hydrobromic acid and 56 μl of bromine, dropwise. After 1 hour at a temperature below 10° C., the solid which separated is collected by filtration and washed on the filter with water. The solid is dried for several hours under vacuum at 50° C., to give 283 mg of the product.
Workup
- customthe solid which separated
- filtrationis collected by filtration
- washwashed on the
- filtrationfilter with water
- customThe solid is dried for several hours under vacuum at 50° C.
Sources & evidence
- ORD record
- ord-2665cb084cde4d90af098c366a82a8bb
- Source dataset
- uspto-grants-2002_10
- Patent number
- US06472396B1
Reaction notes
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