Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 3-(3,4-Dichlorophenyl)-4-hydroxy-1-methylimidazolidin-2-one | HCID 13342322 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13577868 | HCID 13577868 | 82.1% |
Reaction Steps
Dissolved in 100 ml of dimethylformamide was 10.4 g (0.04 mole) of 1-methyl-3-(3,4-dichlorophenyl)-4-hydroxyimidazolidine-2-one. The solution was cooled to 10° C. and 2 g (0.04 mole) of sodium hydride was added to the solution with stirring. After the addition, the mixture was stirred for 30 minutes and 4.4 g of ethyl bromide was added dropwise. The mixture was stirred at room temperature for 2 hours and water was added to the reaction mixture. The mixture was extracted with chloroform and the chloroform extract was concentrated, giving 9.5 g of an oil in 82.1% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04578107 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-c841b01c86304c14844028d3f6d70b76 |
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| Source note | uspto-grants-1986_03 |
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