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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517564Generated: November 4, 2026

Triethylamine → (2-Bromo-3-pyridyl)methyl methanesulfonate

https://huagongshe.com/reaction/1517564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(2-Bromopyridin-3-yl)methanolHCID 14761460—
SolventDichloromethaneHCID 6344—
Product(2-Bromo-3-pyridyl)methyl methanesulfonateHCID 58268552—

Reaction Steps

Triethylamine (8.90 mL) is added to a round bottom flask containing a solution of (2-bromopyridin-3-yl)methanol (8 g, 42.55 mmol) in dichloromethane (212 mL) at 0° C., then methanesulfonyl chloride (3.95 mL) is added and the mixture is stirred at that temperature for 1.5 h. After that time the mixture is washed with water and organic layer is decanted, dried over magnesium sulfate and solvent evaporated under reduced pressure to yield 10.4 g of the title compound used without further purification. MS (m/z): 266, 268 (M+1; M+3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232289B2
Source datasetuspto-grants-2012_07
ORD IDord-593bcd02dce941f9b453c909b64faf74
Source noteuspto-grants-2012_07