HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → (3-Bromo-4-fluorophenyl)(ethyl)sulfane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Bromo-4-Fluorothiophenol | HCID 26597090 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (3-Bromo-4-fluorophenyl)(ethyl)sulfane | HCID 86704956 | 98.5% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A mixture of 3-bromo-4-fluorobenzenethiol (3.89 g, 18.79 mmol) and sodium hydroxide (3.95 mL, 19.73 mmol) in MeOH was stirred at 0° C. for 10 minutes. To this solution was added iodoethane (1.803 mL, 22.54 mmol). The reaction mixture was stirred at ambient temperature for 6 hours. The solvent was removed, and the residue was partitioned between water and ethyl acetate. The aqueous layer was extracted with addition ethyl acetate three times. The combined organic layers were washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated to give the title compound (4.35 g, 18.50 mmol, 98% yield). It was used directly for the next reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09296741B2 |
| Source dataset | uspto-grants-2016_03 |
| ORD ID | ord-20ca365096ac468786d1ce827bda3d91 |
| Source note | uspto-grants-2016_03 |