HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl phenyl sulfoxide → Fluoromethyl phenyl sulfide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl phenyl sulfoxide | HCID 14516 | — |
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Fluoromethyl phenyl sulfide | HCID 5314298 | 86% |
Reaction Steps
To a stirred solution of (methylsulfinyl)benzene (23.0 g, 164 mmol) in chloroform (80 mL) under argon at room temperature was added diethylaminosulfur trifluoride (43.0 mL, 328 mmol) dropwise and the reaction mixture was stirred for 2 days at this temperature then at 60° C. overnight. The mixture was added dropwise to a stirred solution of saturated aqueous sodium hydrogen carbonate at 0° C. then extracted 3 times with dichloromethane. The combined organic layers were dried over sodium sulfate and concentrated to give (fluoromethyl)(phenyl)sulfane (20.0 g, 86%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09266857B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-28ee13892c5548468f0ba414a5345bb9 |
| Source note | uspto-grants-2016_02 |