HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → Diethyl 5-p-toluenesulfonyloxypentylphosphonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Diethyl 5-hydroxypentylphosphonate | HCID 10680635 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | Diethyl 5-p-toluenesulfonyloxypentylphosphonate | HCID 19689184 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
30 g (0.134 mol) of diethyl 5-hydroxypentylphosphonate (see Example 21) were dissolved in 200 ml of pyridine, and the solution was cooled to 0° C. and treated with stirring with 26.1 g (0.134 mol) of 4-toluenesulfonyl chloride. The reaction mixture was concentrated under reduced pressure, taken up in ethyl acetate, washed several times with 20% strength citric acid solution and water and dried over sodium sulfate. After evaporating the solvent, a pale yellow oil remained, which was employed without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05728686 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-6aa4458a36274254b109c6155ed0e1f1 |
| Source note | uspto-grants-1998_03 |