HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 5-Acetyl-4-cyclohexyl-2-methylsulfanyl-thiophene-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Cyclohexyl-3-oxopropanenitrile | HCID 11309597 | — |
| Reactant | Dmf CS2 | HCID 86590990 | — |
| Product | 5-Acetyl-4-cyclohexyl-2-methylsulfanyl-thiophene-3-carbonitrile | HCID 22019043 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06642227B2 |
| Source dataset | uspto-grants-2003_11 |
| ORD ID | ord-29d6a6c76aba42dd88801346e36fbcae |
| Source note | uspto-grants-2003_11 |