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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709702Generated: October 30, 2026

Water → 4-Isobutylthio-2-pyridyl methanesulfonate

https://huagongshe.com/reaction/1709702

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant4-Isobutylthio-2-pyridoneHCID 14072675—
SolventDichloromethaneHCID 6344—
Product4-Isobutylthio-2-pyridyl methanesulfonateHCID 1407253691.6%

Reaction Steps

1.3 g of 4-isobutylthio-2-pyridone (m.p. 119 to 120° C.) and 0.7 ml of methanesulfonyl chloride were dissolved in 10 ml of methylene chloride, and cooled below 10° C. 1.5 ml of triethylamine was added dropwise to the solution with stirring. By stirring at room temperature for 4 hours, the reaction was completed. The reaction solution was poured into 100 ml of water, followed by addition of 100 ml of methylene chloride for separation. The methylene chloride layer was washed with water and saturated aqueous solution of common salt, then distilled to remove the solvent. The obtained residue was purified by silica-gel column chromatography (developer: benzene and n-hexane) to obtain 1.7 g of the objective 4-isobutylthio-2-pyridyl methanesulfonate (yield: 91.6%) as a colourless oil, which were allowed to stand to crystallization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950679
Source datasetuspto-grants-1990_08
ORD IDord-3acee858c2c840ae9d185fc82a070ebd
Source noteuspto-grants-1990_08