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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2010Generated: October 26, 2026

4-Toluenesulfonyl chloride → Diethyl 5-p-toluenesulfonyloxypentylphosphonate

https://huagongshe.com/reaction/2010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDiethyl 5-hydroxypentylphosphonateHCID 10680635—
SolventPyridineHCID 1049—
ProductDiethyl 5-p-toluenesulfonyloxypentylphosphonateHCID 19689184—

Reaction Conditions

Temperature0 °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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728686
Source datasetuspto-grants-1998_03
ORD IDord-6aa4458a36274254b109c6155ed0e1f1
Source noteuspto-grants-1998_03