HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1741007Generated: October 28, 2026
4-Toluenesulfonyl chloride → 4-Methoxy-2-p-toluenesulfonyloxymethylpyridine
https://huagongshe.com/reaction/1741007
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (4-Methoxy-pyridin-2-yl)-methanol | HCID 10820596 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methoxy-2-p-toluenesulfonyloxymethylpyridine | HCID 21834362 | 103.7% |
Reaction Steps
The 2-hydroxymethyl-4-methoxypyridine, (3.48 g, 0.024 mol) was dissolved in 50 ml CH2Cl2 and cooled to 0° C. The p-toluenesulfonyl chloride (5.7 g, 0.03 mol) was added followed by triethylamine (5 g), in 10 ml of CH2Cl2. After 15 minutes, the reaction was stirred at room temperature for one hour. The reaction was diluted with CH2Cl2 (200 ml) and washed with water. The organic layer was separated and dried with MgSO4, filtered and concentrated to afford 7.3 g of crude subtitle compound suitable for further use.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05972972 |
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| Source dataset | uspto-grants-1999_10 |
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| ORD ID | ord-529afc0034b9436f8c06c3d3605ef849 |
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| Source note | uspto-grants-1999_10 |
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