HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 1-Bromo-2-ethylsulfanyl-4-trifluoromethylsulfanylbenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium ethanethiolate | HCID 4459711 | — |
| Reactant | 4-Bromo-3-fluorophenyl trifluoromethyl sulphide | HCID 118035676 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Bromo-2-ethylsulfanyl-4-trifluoromethylsulfanylbenzene | HCID 118035563 | 58.3% |
Reaction Steps
0.21 g of sodium ethanethiolate (80%) was added to a mixture of 0.55 g of l-bromo-2-fluoro-4-trifluoromethylsulfanylbenzene and 4 ml of THF under ice cooling, and the mixture was stirred at room temperature for 30 minutes. 2 mL of DMF was added to the reaction mixture, and the mixture was stirred at 80° C. for 2 hours. A saturated aqueous sodium bicarbonate solution was added to the cooled reaction mixture, and the mixture was extracted with ethyl acetate and then dried with anhydrous sodium sulfate. The mixture was concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 0.37 g of 1-bromo-2-ethylsulfanyl-4-trifluoromethylsulfanylbenzene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156838B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-09172ec6784f44fda24172d803031bb5 |
| Source note | uspto-grants-2015_10 |