Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1906462Generated: November 2, 2026

Water → HCID 13823485, compound

https://huagongshe.com/reaction/1906462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 178477276HCID 178477276—
SolventDichloromethaneHCID 6344—
ProductHCID 13823485HCID 1382348593.5%

Reaction Conditions

Temperature40 °C

Reaction Steps

5 g of 3-chloro-6-ethylthio-2-pyridinol and 3.7 g of methanesulfonyl chloride were dissolved in 50 ml of methylene chloride, followed by stirring. 4 g of triethylamine was added dropwise to the solution at 10° C. or below and the obtained mixture was allowed to stand to lower the temperature to room temperature. The mixture was heated to 40° C. and stirred for 2 hours. 50 ml of chilled water was poured into the reaction mixture to separate the methylene chloride layer. The water layer was further extracted with 50 ml of methylene chloride. The obtained methylene chloride layer was combined with the above methylene chloride layer. The combined layer was washed with water and distilled to remove the solvent. The obtained residue was purified by silica gel column chromatography (with toluene and n-hexane) to obtain 6.6 g of objective 3-chloro-6-ethylthio-2-pyridyl methanesulfonate as a colorless crystal (yield: 93.4%). m.p. 40° to 41° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04652574
Source datasetuspto-grants-1987_03
ORD IDord-61eebcc5f7084e0a9603d9740949dae3
Source noteuspto-grants-1987_03