HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059525Generated: October 31, 2026
Potassium Iodide → 3-Hydroxypropyl 4-methylbenzenesulfonate
https://huagongshe.com/reaction/2059525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | 1,3-Propanediol | HCID 10442 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Hydroxypropyl 4-methylbenzenesulfonate | HCID 11961356 | 53.5% |
Reaction Steps
1.45 mL (corresponding to 20.0 mmol) of 1,3-propanediol was dissolved in 200 mL of methylene chloride. To this solution under an ice bath, 6.96 g (corresponding to 30.0 mmol) of silver oxide, 666 mg (corresponding to 4.0 mmol) of potassium iodide and 4.21 g (corresponding to 22.0 mmol) of p-toluenesulfonyl chloride were added. The resulting mixture was stirred at room temperature for 3 hours. Insoluble matters were filtered out of the reaction mixture, and were washed with ethyl acetate. The washings were combined with the filtrate, and the mixture was concentrated. The resulting crude product was purified with flash silica gel column chromatography (elution solvent: hexane/ethyl acetate=3/2 to 1/1) to obtain 2.47 g (corresponding to 10.7 mmol) of 1,3-propanediol mono-p-toluenesulfonate (FIG. 1, Step 6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08277777B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-c4118500adee4f2098228f0201e4ab83 |
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| Source note | uspto-grants-2012_10 |
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