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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010993Generated: October 30, 2026

Triethylamine → Oxan-4-ylmethyl methanesulfonate

https://huagongshe.com/reaction/1010993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(Oxan-4-yl)methanolHCID 2773573—
SolventDichloromethaneHCID 6344—
ProductOxan-4-ylmethyl methanesulfonateHCID 15166436—

Reaction Steps

To tetrahydro-2H-pyran-4-ylmethanol (6.2 g) in dry dichloromethane (226.3 ml) at 0° C. and under nitrogen, was added triethylamine (18.1 ml), followed by mesyl chloride (5.4 ml). The reaction was allowed to warm to room temperature and left at this temperature overnight. The reaction mixture was washed with saturated aqueous sodium bicarbonate (200 ml). The organic layer was separated, passed through a hydrophobic frit to dry and concentrated in vacuo to yield a light brown lumpy solid (10.17 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977344B2
Source datasetuspto-grants-2011_07
ORD IDord-1c79bcc0a48f4c788f711db359048136
Source noteuspto-grants-2011_07