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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1903386Generated: October 25, 2026

Tetraethylene Glycol → 1,11-Bis(methanesulfonyloxy)-3,6,9-trioxandecane

https://huagongshe.com/reaction/1903386

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetraethylene GlycolHCID 8200—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventWaterHCID 962—
Product1,11-Bis(methanesulfonyloxy)-3,6,9-trioxandecaneHCID 363787590%

Reaction Conditions

Temperature5 °C

Reaction Steps

A 5,000 mL, 3-necked flask equipped with a mechanical stirrer, thermometer and 500 mL addition funnel was charged with tetraethylene glycol (388 g, 2.0 mol) dichloromethane (1,500 mL) and triethylamine (445 g, 4.40 mol). The mixture was stirred and cooled to ca. 5° C., and methanesulfonyl chloride (470 g, 4.1 mol) was added dropwise over 3 hours. The reaction mixture was stirred an additional 3 hours while warming to 25° C., then water (1,000 mL) was added and the phases were separated. The organic layer was washed with ice-cold 6 N HCl (2×1,000 mL) and then washed with 5% Na2CO3, saturated aqueous NaCl, dried, filtered and evaporated in vacuo to yield 627 g (90%) of tetraethylene glycol dimesylate, i.e.,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04436664
Source datasetuspto-grants-1984_03
ORD IDord-d18027070c704b96bb52063f604f8596
Source noteuspto-grants-1984_03