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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258423Generated: October 31, 2026

4-Toluenesulfonyl chloride → 2-(Benzyloxy)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/258423

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-(Benzyloxy) ethanolHCID 12141—
ReactantSodium hydrideHCID 24758—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(Benzyloxy)ethyl 4-methylbenzenesulfonateHCID 56137578.3%

Reaction Steps

To a slurry of sodium hydride (0.4 g,17 mmol) in 20 ml ethylene glycol dimethyl ether cooled with an ice bath under an atmosphere of nitrogen, a solution of 2-benzyloxyethanol (2.1 ml, 15 mmol) and p-toluene sulfonyl chloride (2.9 g, 15 mmol) in ethylene glycol dimethyl ether was added dropwise. When the addition was complete, the ice bath was removed and the solution stirred at room temperature for 18 hours. After dilution with diethyl ether, the resulting slurry was filtered through anhydrous magnesium sulfate and concentrated under vacuum to yield 3.6 g of crude 2-benzyloxyethyl p-toluenesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05266722
Source datasetuspto-grants-1993_11
ORD IDord-f5e8f4949dc14dcea337fddbd0ef2f51
Source noteuspto-grants-1993_11