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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1584503Generated: November 2, 2026

Isopropylethanediol → 2-Isopropoxyethyl Methanesulfonate

https://huagongshe.com/reaction/1584503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylethanediolHCID 7996—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
SolventDichloromethaneHCID 6344—
Product2-Isopropoxyethyl MethanesulfonateHCID 18465045—

Reaction Steps

Combine 2-isopropoxyethanol (1.0 g, 9.6 mmol), N,N-diisopropylethylamine (2.73 g, 21.12 mmol), and dichloromethane (20 mL). Cool in an ice bath. Add dropwise methanesulfonyl chloride (1.43 g, 9.6 mmol). After 2 hours, dilute the reaction mixture with dichloromethane and extract with 1M hydrochloric acid solution, a saturated solution of sodium bicarbonate, and then brine. Dry the organic layer over Na2SO4, filter, and evaporate in vacuo to give a residue. Distill the residue to give 2-(isopropoxy)ethyl mesylate: bp; 84° C. at 0.1 mm Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05932571
Source datasetuspto-grants-1999_08
ORD IDord-e201e4c21747414680568c5ad563141b
Source noteuspto-grants-1999_08