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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703048Generated: October 30, 2026

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

https://huagongshe.com/reaction/703048

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

An example is disclosed in U.S. patent application Ser. No. 269,205. 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 numberUS04981648
Source datasetuspto-grants-1991_01
ORD IDord-3d2385f3820147558e8bff3be2197ac7
Source noteuspto-grants-1991_01