Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Diethyl bromomalonate | HCID 69637 | — |
| Reactant | 5-(2-Chloro-4-trifluoromethylphenoxy)-2-nitrophenol | HCID 162064 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19008600 | HCID 19008600 | — |
Reaction Steps
To a suspension of 60% sodium hydride (0.4 g) in DMF (5 ml) was dropwise added, under ice-cooling, a DMF (5 ml) solution of 5-(2-chloro-4-trifluoromethylphenoxy)-2-nitrophenol (3.3 g), and the mixture was stirred for 10 minutes. To the solution was added diethyl bromomalonate (2.1 ml), and the mixture stirred at 70° C. for 30 minutes. Then, to the reaction mixture was added water (10 ml), and the mixture extracted twice with ethyl acetate (20 ml). The extract was washed with water and then with saturated aqueous sodium chloride, and dried over magnesium sulfate. The solvent was evaporated under a reduced pressure, and the residue was purified by silica gel chromatography (eluant: n-hexane/ethyl acetate=5/1) to give 3.0 g of the title compound (colorless oil). Also, 0.7 g of the phenol derivative of the starting material was recovered.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05338719 |
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| Source dataset | uspto-grants-1994_08 |
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| ORD ID | ord-2061f26ed9c54b9bbc9aa039ea1f0979 |
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| Source note | uspto-grants-1994_08 |
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