HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thiophenol → HCID 20069003, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thiophenol | HCID 7969 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(3,5-DiCyanothienyl) ethyl sulfoxide | HCID 23273758 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 20069003 | HCID 20069003 | — |
Reaction Steps
4.4 ml of thiophenol and 5.0 ml of triethylamine are added, while stirring, to a solution of 8.9 g of 2-ethylsulphinyl-3,5-dicyanothiophene, obtained according to Example I, in 100 ml of acetonitrile. After leaving to stand overnight, the reaction mixture is refluxed for 8 hours. After evaporating the solvent, the residue is taken up in methylene chloride and chromatographed over a 1 l dry silica gel column. The desired product is obtained in a yield of 9.07 g; melting-point 68°-71° C. Optionally, any 2-alkylsulphinyl compound may be used as the starting substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04994485 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-6d235710006e4d1fbca6e6926b8ab348 |
| Source note | uspto-grants-1991_02 |