Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13232347 | HCID 13232347 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13232348 | HCID 13232348 | 82.5% |
Reaction Steps
6.2 g of imidazole and 1.3 g of sodium hydride (50% strength dispersion in mineral oil) were dispersed in 50 ml of N,N-dimethylformamide, and a solution of 12 g of 2-bromomethyl-2-(4-chlorophenyl)-3-(2,4-dichlorophenyl)-oxirane (isomer B) and 5 g of potassium iodide in 50 ml of N,N-dimethylformamide was added at room temperature (20° C.). After 8 hours, the reaction solution was poured onto water and the mixture was extracted with ethyl acetate. The organic phase was washed with water and dried over sodium sulfate, the solvent was evaporated off under reduced pressure and the residue was recrystallized from diisopropyl ether. 9.4 g (82.5%) of 2-(1H-imidazol-1-yl-methyl)-2-(4-chlorophenyl)-3-(2,4-dichlorophenyl)-oxirane (isomer B) of melting point 109° C. were obtained (compound 2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04464381 |
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| Source dataset | uspto-grants-1984_08 |
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| ORD ID | ord-5c00229d9ada4f7f978248b74411cc68 |
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| Source note | uspto-grants-1984_08 |
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