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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025285Generated: October 31, 2026

Methanesulfonyl chloride → HCID 46901655, compound

https://huagongshe.com/reaction/1025285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Cyano-5-hydroxymethylpyridineHCID 12251966—
SolventDichloromethaneHCID 6344—
ProductHCID 46901655HCID 4690165592.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-(hydroxymethyl)picolinonitrile (1.59 g, 11.9 mmol) in 80 mL of DCM was added diisopropylethylamine (3.2 mL), followed by a solution of methanesulfonyl chloride (1.49 g, 13.0 mmol) in 20 mL of DCM at 0° C. The solution was stirred at 0° C. for 40 min and washed with 5% citric acid, sat. NaHCO3 (aq.) and brine. After concentration, the residue was purified by silica gel chromatography (elution with 0-30% EtOAc/Hex) to afford (6-cyanopyridin-3-yl)methyl methanesulfonate (2.33 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729071B2
Source datasetuspto-grants-2014_05
ORD IDord-daa254e941e34708a31a4e1185b5d19b
Source noteuspto-grants-2014_05