Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010983Generated: October 29, 2026

Triethylamine → 2-(Oxan-2-yl)ethyl methanesulfonate

https://huagongshe.com/reaction/1010983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant2-(Oxan-2-yl)ethan-1-olHCID 13948128—
SolventDichloromethaneHCID 6344—
Product2-(Oxan-2-yl)ethyl methanesulfonateHCID 57699828110%

Reaction Steps

2-(Tetrahydro-2H-pyran-2-yl)ethanol (465 mg) was dissolved in dry DCM (10 mL) and triethylamine (996 mg) was added. The stirred solution was cooled in an ice bath under nitrogen and methanesulphonyl chloride (359 mg) was added dropwise over 5 mins. The reaction was allowed to warm to room temperature as the ice bath melted and was left for 16 h. The mixture was then shaken with saturated sodium bicarbonate solution and the aqueous layer was extracted with DCM (×2). The combined organic extracts were washed with brine, dried using a hydrophobic frit and evaporated to give the title compound as a brown oil (718 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977344B2
Source datasetuspto-grants-2011_07
ORD IDord-355400d2f3d942ef96adb9d895679797
Source noteuspto-grants-2011_07