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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341041Generated: October 30, 2026

Triethylamine → (5-Bromo-3-fluoropyridin-2-yl)methyl methanesulfonate

https://huagongshe.com/reaction/341041

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(5-Bromo-3-fluoropyridin-2-yl)methanolHCID 57416937—
SolventDichloromethaneHCID 6344—
Product(5-Bromo-3-fluoropyridin-2-yl)methyl methanesulfonateHCID 86668676—

Reaction Conditions

Temperature0 °C

Reaction Steps

(5-Bromo-3-fluoropyridin-2-yl)methanol (0.20 g, 0.99 mmol) was dissolved in dichloromethane (5 mL), cooled to 0° C. and treated with triethylamine (0.15 mL, 1.1 mmol, 1.1 equiv) and methanesulfonyl chloride (0.085 mL, 1.1 mmol, 1.1 equiv). After 15 minutes, the mixture was diluted with dichloromethane (100 mL) and washed once with sodium bicarbonate (20 mL, aqueous saturated) and brine (50 mL), dried with sodium sulfate, filtered and concentrated in vacuo, providing the titled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895580B2
Source datasetuspto-grants-2014_11
ORD IDord-66f59257680747539b5e9c98e033cd70
Source noteuspto-grants-2014_11