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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1632292Generated: October 25, 2026

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

https://huagongshe.com/reaction/1632292

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 6N 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 numberUS04474963
Source datasetuspto-grants-1984_10
ORD IDord-1ed64e83f3564e9fba332dad884dd8db
Source noteuspto-grants-1984_10