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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTriethylamineHCID 8471—
Reactant(4-Methoxy-pyridin-2-yl)-methanolHCID 10820596—
SolventDichloromethaneHCID 6344—
Product4-Methoxy-2-p-toluenesulfonyloxymethylpyridineHCID 21834362103.7%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05972972
Source datasetuspto-grants-1999_10
ORD IDord-529afc0034b9436f8c06c3d3605ef849
Source noteuspto-grants-1999_10