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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1753685Generated: October 28, 2026

4-Toluenesulfonyl chloride → HCID 11076628, compound

https://huagongshe.com/reaction/1753685

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantTetrahydrofuranHCID 8028—
ReactantDiethylene Glycol Monomethyl EtherHCID 8134—
ReactantSodium HydroxideHCID 14798—
SolventWaterHCID 962—
ProductHCID 11076628HCID 11076628101.7%

Reaction Steps

Under ice cooling, a mixture of 515 g of p-toluenesulfonyl chloride and 500 ml of THF was added dropwise to a mixture of 295 g of 2-(2-methoxyethoxy)ethanol, 589 g of 25 wt % NaOH aqueous solution, and 2,500 ml of THF. The reaction solution was aged for 1.5 hours, after which 1,500 ml of water was added to quench the reaction. The organic layer was separated and concentrated in vacuum. The concentrate was dissolved in a mixture of 660 ml toluene and 330 ml hexane, and washed with water. The organic layer was concentrated in vacuum, obtaining 684.74 g of the target compound, 2-(2-methoxyethoxy)ethyl p-toluenesulfonate as oily matter. Yield 97%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09164384B2
Source datasetuspto-grants-2015_10
ORD IDord-2036542604194db1a90de657546d519e
Source noteuspto-grants-2015_10