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Methyl iodide → 5-Acetyl-4-cyclohexyl-2-methylsulfanyl-thiophene-3-carbonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Methyl iodide | HCID 6328 | — |
| 反応物 | Chloroacetone | HCID 6571 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 3-Cyclohexyl-3-oxopropanenitrile | HCID 11309597 | — |
| 反応物 | Dmf CS2 | HCID 86590990 | — |
| 生成物 | 5-Acetyl-4-cyclohexyl-2-methylsulfanyl-thiophene-3-carbonitrile | HCID 22019043 | — |
反応手順
To a solution of 3-cyclohexyl-3-oxo-propionitrile in DMF:CS2 (1:1) was added K2CO3 at 0° C. and the reaction mixture stirred at ambient temperature for 2 hours. To the resulting reaction mixture was added chloroacetone (1 equivalent) and the reaction mixture stirred at ambient temperature for 3 hours. Iodomethane was then added and the resulting mixture was stirred at ambient temperature overnight. The reaction mixture was partitioned between ethyl acetate and brine, the organic phase dried with MgSO4 and the solvent was removed under reduced pressure. The crude product was purified by silica gel chromatography.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07084159B2 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-183102cc420b4877ac00ee09af6bc6a9 |
| 出典メモ | uspto-grants-2006_08 |