HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → 2-Methylthio-3,5-dicyano-4-methoxythiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Methylthio-3,5-dicyano-4-hydroxythiophene | HCID 14119770 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Methylthio-3,5-dicyano-4-methoxythiophene | HCID 14119771 | — |
Reaction Steps
6 g of 2-methylthio-3,5-dicyano-4-hydroxythiophene 10 ml of methyl iodide, 10 g of potassium carbonate, and 3 ml of triethylamine are refluxed in 300 ml of acetonitrile while stirring. After 2 hours the reaction mixture is filtered warm and evaporated to dryness. The residue is taken up in 200 ml of methylene chloride and washed successively with a solution of potassium carbonate in water and with water. The methylene chloride solution is then dried and evaporated to dryness. After recrystallisation of the residue from isopropanol, the desired product is obtained in a yield of 4.0 g; melting-point 132° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04994485 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-0887362eb0574398a66fd717bf5a366f |
| Source note | uspto-grants-1991_02 |