Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178475917 | HCID 178475917 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22130798 | HCID 22130798 | 46.6% |
Reaction Steps
In 12 ml of dry dimethylformamide was dissolved 600 mg (1.4 mmol)of [2-t-butyldimethylsilyloxymethyl-5-(3-chlorophenylthio)-1H-imidazol-4-yl]methyl acetate, followed by addition of anhydrous potassium carbonate (2.8 mmol). Then, 240 mg (1.7 mmol)of methyl iodide was added, and the reaction mixture was stirred at room temperature for 1 hour. To the reaction mixture, ice-water was added, extracted with diethyl ether, the organic layer was washed with water and dried over sodium sulfate. The solvent was distilled off under reduced pressure, and the residue was purified by silica gel chromatography (ethyl acetate:n-hexane=1:2)to obtain 288 mg of [2-t-butyldimethylsilyloxymethyl-5-(3-chlorophenylthio)-1-methyl-1H-imidazol-4-yl]methyl acetate (47)as oil (yield 46%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05910506 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-46024d429cc14fe8b1af601bdecc37f9 |
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| Source note | uspto-grants-1999_06 |
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