HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1018658Generated: October 26, 2026
4-Toluenesulfonyl chloride → 3-Phenylprop-2-yn-1-yl 4-methylbenzene-1-sulfonate
https://huagongshe.com/reaction/1018658
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 3-Phenyl-2-propyn-1-ol | HCID 123115 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-Phenylprop-2-yn-1-yl 4-methylbenzene-1-sulfonate | HCID 10517333 | — |
Reaction Steps
25 g of 3-phenyl-2-propyn-1-ol and 40 g of toluene-4-sulfonic acid chloride are dissolved in 500 ml of diethyl ether and cooled to −20° C. 26.6 g of finely powdered potassium hydroxide are added in portions to that solution, over a period of 20 minutes, in such a manner that the internal temperature of the reaction mixture does not exceed −5° C. When the addition is complete, the reaction mixture is stirred for 2 hours at from 0 to 5° C. and then introduced into one litre of ice-water. Extraction is carried out twice using one litre of diethyl ether each time. The organic phases are washed once with 500 ml of saturated sodium chloride solution, combined, dried over sodium sulfate and concentrated, yielding toluene-4-sulfonic acid (3-phenyl-2-propyn-1-yl) ester in the form of a colourless resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06482859B1 |
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| Source dataset | uspto-grants-2002_11 |
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| ORD ID | ord-6fc67138dea34198a7936b627073960a |
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| Source note | uspto-grants-2002_11 |
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