HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 23157571, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethane, 1-chloro-2-ethoxy- | HCID 12341 | — |
| Reactant | 3,5-Dimethylbenzenethiol | HCID 117548 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23157571 | HCID 23157571 | 76.2% |
Reaction Steps
To a solution of 1-chloro-2-ethoxyethane (5.90 mL, 54.3 mmol) and 3,5-dimethylbenzenethiol (5.00 g, 36.2 mmol) in N,N-dimethylformamide (140 mL) were added potassium carbonate (5.50 g, 39.8 mmol) and potassium iodide (0.90 g, 5.43 mmol) under stirring at room temperature, and the mixture was stirred at 80° C. for 5 hr. The reaction mixture was concentrated under reduced pressure, and water was added to the residue. The mixture was extracted with diethyl ether. The extract was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-hexane/ethyl acetate=10/1) to give the title compound (5.80 g, yield 76%) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07786165B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-6ebf4fee7c7f4429b6d28bee9379eac0 |
| Source note | uspto-grants-2010_08 |