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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1467962Generated: October 25, 2026

Triethylamine → (2-Chloropyridin-4-yl)methyl methanesulfonate

https://huagongshe.com/reaction/1467962

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(2-Chloropyridin-4-yl)methanolHCID 7062237—
SolventDichloromethaneHCID 6344—
Product(2-Chloropyridin-4-yl)methyl methanesulfonateHCID 5343676468.4%

Reaction Steps

To a stirred solution of (2-chloropyridin-4-yl)methanol (0.500 g, 3.496 mmol) in dichloromethane (15 mL), triethylamine (0.424 g, 4.195 mmol) and methanesulfonylchloride (0.440 g, 3.846 mmol) were added at 0° C. and stirred at room temperature for 2-3 h. The reaction was quenched with water and extracted with dichloromethane. The organic layer was concentrated in vacuo to give (2-chloropyridin-4-yl)methyl methanesulfonate (0.530 g, 68%); MS: 221.9 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000175B2
Source datasetuspto-grants-2015_04
ORD IDord-dbe6dcafa19e4fc0b55dd62ddede6b56
Source noteuspto-grants-2015_04