HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Chloride → 1-(Ethylsulfanyl)-4-nitrobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Chloride | HCID 5234 | — |
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4-Nitrobenzenethiol | HCID 15809 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(Ethylsulfanyl)-4-nitrobenzene | HCID 12321339 | 86.2% |
Reaction Steps
16.56 g (106.72 mmol) of 4-nitrothiophenol was added, while cooling with water, to a solution of 4.27 g (106.76 mmol) sodium hydroxide in 320 ml ethanol and it was stirred for 15 minutes at room temperature. Then, while cooling with water, 8.63 ml (106.79 mmol) of ethyl iodide was added and the mixture was stirred overnight at room temperature. The mixture was added to saturated sodium chloride solution and was extracted with ethyl acetate (2×). The combined organic phases were dried (Na2SO4), filtered and concentrated by evaporation. Then it was dissolved in DCM and filtered again and evaporated to dryness. 16.86 g (92.02 mmol) of the raw product was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08735412B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-298dec004d194a428acb527faaae0ef4 |
| Source note | uspto-grants-2014_05 |