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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1366348Generated: October 30, 2026

Triethylamine → (2R)-1,4-dioxan-2-ylmethyl methanesulfonate

https://huagongshe.com/reaction/1366348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(S)-(1,4-Dioxan-2-yl)methanolHCID 44429359—
SolventDichloromethaneHCID 6344—
Product(2R)-1,4-dioxan-2-ylmethyl methanesulfonateHCID 86609782—

Reaction Conditions

Temperature-10 °C

Reaction Steps

A round bottomed flask was charged with (2S)-1,4-dioxan-2-ylmethanol (115 mg, 0.973 mmol), triethylamine (0.204 mL, 1.46 mmol), and 5 mL of dichloromethane then cooled to −10° C. Methanesulfonyl chloride (91 μL, 1.17 mmol) was added by syringe and the solution was stirred for 30 minutes at −10° C. The solution was diluted in dichloromethane, washed with 1 M HCl, and the aqueous layer was extracted with dichloromethane (2×). The combined organic layers were washed with saturated aquoues sodium bicarbonate (2×) and brine, then dried over sodium sulfate and concentrated to afford (2R)-1,4-dioxan-2-ylmethyl methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07893081B2
Source datasetuspto-grants-2011_02
ORD IDord-c18f343f842d47d6bff2ea7b5a867537
Source noteuspto-grants-2011_02