Water → HCID 21536165, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([N:9]([OH:13])[C:10]([NH2:12])=[O:11])[CH:5]=[CH:6][C:7]=1[F:8].Cl[C:15](OCC)=[O:16].O>[OH-].[Na+]>[F:1][C:2]1[CH:3]=[C:4]([N:9]2[C:10](=[O:11])[NH:12][C:15](=[O:16])[O:13]2)[CH:5]=[CH:6][C:7]=1[F:8]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1-(3,4-Difluorophenyl)-1-hydroxyurea (0.2 mole) dissolved in aqueous sodium hydroxide (200 ml; 2N) is charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The solution is cooled to a temperature of about 10°C and ethyl chloroformate (0.21 mole) is slowly added with stirring. After the addition is completed stirring is continued for a period of about one hour. The reaction mixture is then poured into 2 liters of water. The resulting aqueous solution is then filtered and the filtrate is cooled and acidified with concentrated hydrochloric acid to form a precipitate. The precipitate is recovered by filtration and is dried. The dried product is then dissolved in a methylene chloride-tetrahydrofuran mixture and the resulting solution is dried over anhydrous magnesium sulfate, filtered and stripped of solvent to yield the desired product 2-(3,4-difluorophenyl)-1,2,4-oxadiazolidin-3,5-dione as the residue.
Workup
- additionis charged into a glass reaction vessel
- customequipped with a mechanical stirrer
- additionis slowly added
- additionAfter the addition
- stirringis completed stirring
- filtrationThe resulting aqueous solution is then filtered
- temperaturethe filtrate is cooled
- customto form a precipitate
- filtrationThe precipitate is recovered by filtration
- customis dried
- dissolutionThe dried product is then dissolved in a methylene chloride-tetrahydrofuran mixture
- dry with materialthe resulting solution is dried over anhydrous magnesium sulfate
- filtrationfiltered
Sources & evidence
- ORD record
- ord-3f1192254f0242b59edd81775cce6600
- Source dataset
- uspto-grants-1976_05
- Patent number
- US03959478
Reaction notes
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