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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033917Generated: November 1, 2026

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

https://huagongshe.com/reaction/1033917

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 numberUS05312953
Source datasetuspto-grants-1994_05
ORD IDord-f1b588720ef74b4bb87e1e9da5f0b2c2
Source noteuspto-grants-1994_05