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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243769Generated: October 27, 2026

Chloride → 2-(2-(2-Methoxyethoxy)ethoxy)ethyl methanesulfonate

https://huagongshe.com/reaction/1243769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
ReactantTriethylene glycol monomethyl etherHCID 8178—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
SolventDichloromethaneHCID 6344—
Product2-(2-(2-Methoxyethoxy)ethoxy)ethyl methanesulfonateHCID 12621272—

Reaction Steps

A solution of non-polydispersed triethylene glycol monomethyl ether molecules (4.00 mL, 4.19 g, 25.5 mmol) and triethylamine (4.26 mL, 3.09 g, 30.6 mmol) in dry dichloromethane (50 mL) was chilled in an ice bath and place under a nitrogen atmosphere. A solution of methanesulfonyl chloride (2.37 mL, 3.51 g, 30.6 mmol) in dry dichloromethane (20 mL) was added dropwise from an addition funnel. Ten minutes after the completion of the chloride addition, the reaction mixture was removed from the ice bath and allowed to come to room temperature. The mixture was stirred for an additional hour, at which time TLC (CHCl3 with 15% MeOH as the elutant) showed no remaining triethylene glycol monomethyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119162B2
Source datasetuspto-grants-2006_10
ORD IDord-5d3d3d6bfde9438b89e9e2e33219cb8e
Source noteuspto-grants-2006_10