HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742607Generated: October 29, 2026
4-Toluenesulfonyl chloride → (5-Ethyl-2-pyridyl)ethane p-toluenesulfonate
https://huagongshe.com/reaction/742607
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | (5-Ethyl-2-pyridyl)ethanol | HCID 19426344 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5-Ethyl-2-pyridyl)ethane p-toluenesulfonate | HCID 19426348 | 93.2% |
Reaction Steps
7.1 g of sodium hydroxide was dissolved in 33 ml of water, and 7.6 g of (5-ethyl-2-pyridyl)ethanol was dissolved in 33 ml of tetrahydrofuran. Both solutions were mixed and cooled. To the resultant solution was added dropwise gradually at 0° C. a solution of 11.7 g of p-toluenesulfonyl chloride in 51 ml of tetrahydrofuran, followed by stirring for 2 hours at the same temperature. To the reaction mixture was added ice water. The mixture was extracted twice with 100 ml each of methylene chloride. The extracted organic layers are combined. The resultant organic layer was washed with water and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, whereby 14.4 g of (5-ethyl-2-pyridyl)ethane p-toluenesulfonate was obtained as a pale yellow oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05554758 |
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| Source dataset | uspto-grants-1996_09 |
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| ORD ID | ord-e41048f6d0ef4cb9afce8798ae72002a |
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| Source note | uspto-grants-1996_09 |
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