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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033916Generated: October 31, 2026

1,2-Dimethoxyethane → 2-(Benzyloxy)ethyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/1033916

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
Reactanto-Toluenesulfonyl chlorideHCID 8623—
Reactant2-(Benzyloxy) ethanolHCID 12141—
ReactantSodium hydrideHCID 24758—
Product2-(Benzyloxy)ethyl 4-methylbenzenesulfonateHCID 561375—

Reaction Steps

The 2-benzyloxyalkyl p-toluenesulfonate used in step (a) may be prepared by conventional techniques from commercially available material. For example, a solution of 2-benzyloxyethanol and toluene sulfonyl chloride may be added to a slurry of sodium hydride in ethylene glycol dimethyl ether cooled (e.g. using an ice bath) under a nitrogen atmosphere. After the addition, the mixture is warmed and allowed to react at room temperature. Crude 2-benzyloxyethyl p-toluenesulfonate may be obtained from the reaction mixture by diluting the mixture with diethyl ether, filtering the diluted mixture through anhydrous magnesium sulfate, and concentrating the filtered product under vacuum.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312953
Source datasetuspto-grants-1994_05
ORD IDord-fd87504a38ea48058c034c07d3569af7
Source noteuspto-grants-1994_05