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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2414852Generated: October 26, 2026

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

https://huagongshe.com/reaction/2414852

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 numberUS06815530B2
Source datasetuspto-grants-2004_11
ORD IDord-a9b2d3d0c83a41a084638da0f28ba858
Source noteuspto-grants-2004_11