Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 594968Generated: October 30, 2026

Triethylamine → (2-Fluoropyridin-3-yl)methyl methanesulfonate

https://huagongshe.com/reaction/594968

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Fluoro-3-(hydroxymethyl)pyridineHCID 14761461—
SolventDichloromethaneHCID 6344—
Product(2-Fluoropyridin-3-yl)methyl methanesulfonateHCID 86634652—

Reaction Steps

A solution of (2-fluoropyridin-3-yl)methanol (400 mg, 3.1 mmol), methanesulfonyl chloride (0.37 mL, 4.7 mmol) and triethylamine (0.88 mL, 6.30 mmol) in dichloromethane (10 mL) was stirred at rt for 16 h. The mixture was then diluted with dichloromethane and washed with H2O, then brine. The organic phase was collected, dried (MgSO4) and concentrated in vacuo to give (2-fluoropyridin-3-yl)methyl methanesulfonate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242987B2
Source datasetuspto-grants-2016_01
ORD IDord-5fb0a970e0324ed3a251cb256e4adeca
Source noteuspto-grants-2016_01