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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220394Generated: October 26, 2026

Isopropylethanediol → 2-Isopropoxyethyl Methanesulfonate

https://huagongshe.com/reaction/220394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropylethanediolHCID 7996—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product2-Isopropoxyethyl MethanesulfonateHCID 18465045126.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

A round bottom flask was charged with 2-isopropoxyethanol (0.5 mL, 4.34 mmol) and dichloromethane (21.68 mL) and was cooled to 0° C. Triethylamine (1.208 mL, 8.67 mmol) was added along with a tip of DMAP. Methanesulfonyl chloride (0.338 mL, 4.34 mmol) was added dropwise. The reaction mixture was slowly warmed to rt over 2 h. The reaction mixture was quenched with saturated aqueous ammonium chloride and transferred to a separatory funnel. The aqueous layer was extracted with dichloromethane (2×). The combined organics were washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. 2-Isopropoxyethyl methanesulfonate (1 g) was isolated as a clear oil and was immediately used in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202881B2
Source datasetuspto-grants-2012_06
ORD IDord-5dd2a2d8c64b4e20b81cc5e9e4f85b5f
Source noteuspto-grants-2012_06