Sodium Hydroxide → 5-Phenyloxazolidine-2,4-dione
Reaction equation
[OH:1][C:2]1([C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)C(=O)N[C:5](=[O:9])[NH:4][C:3]1=[O:10].[OH-].[Na+]>>[C:11]1([CH:2]2[O:1][C:5](=[O:9])[NH:4][C:3]2=[O:10])[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1Participants
3
Procedure
5-Hydroxy-5-phenyl-2,4,6(1H,3H,5H)-pyrimidinetrione (0.7 g.) is dissolved in 15 ml. of 1 N sodium hydroxide, stirred at room temperature for 15 minutes, extracted with ethyl acetate, made slightly acidic with about 1 ml. of glacial acetic acid, and extracted with 25 ml. of ethyl acetate. The latter ethyl acetate extract is back washed with about 6.5 ml. of water, filtered over a bed of anhydrous magnesium sulfate and evaporated to yield 5-phenyloxazolidine-2,4-dione.
Workup
- extractionextracted with ethyl acetate
- extractionof glacial acetic acid, and extracted with 25 ml
- extractionThe latter ethyl acetate extract
- washis back washed with about 6.5 ml
- filtrationof water, filtered over a bed of anhydrous magnesium sulfate
- customevaporated
Sources & evidence
- ORD record
- ord-e2c5061a1a1b47c3ba2cfd058ef8e5a7
- Source dataset
- uspto-grants-1983_01
- Patent number
- US04367234
Reaction notes
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