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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622633Generated: October 31, 2026

1-Methyl-2-oxo-3-piperidinyl methanesulfonate → 1-Methylpiperidin-2-on-3-yl Thioacetate

https://huagongshe.com/reaction/622633

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methyl-2-oxo-3-piperidinyl methanesulfonateHCID 14456895—
ReactantPotassium ethanethioateHCID 23670855—
SolventAcetoneHCID 180—
Product1-Methylpiperidin-2-on-3-yl ThioacetateHCID 2129136840.1%

Reaction Steps

A mixture of 1-methyl-2-oxo-3-piperidinyl methanesulfonate (1.7 g., 0.008 mole) and potassium thioacetate (1.39 g., 0.012 mole) in 80 ml. acetone was refluxed under nitrogen for 20 hours. The reaction mixture was concentrated in vacuo and the residue was dissolved in 50 ml. ethyl acetate and 50 ml. water. The ethyl acetate layer was washed with 50 ml. water and 50 ml saturated aqueous sodium chloride solution, dried over anhydrous sodium acetate and concentrated in vacuo. The residue was chromatographed on silica gel eluting with ethyl acetate to yield 600 mg (40% yield) of the title compound. NMR (CDCl3): 1.7-2.5 (c) and 2.38 (s) (total 7H); 3.0 (s, 3H); 3.36 (m, 2H); and 4.2 (m, 1H)ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04772597
Source datasetuspto-grants-1988_09
ORD IDord-17531dad62b94a8ab6a355cc6eaf3a9f
Source noteuspto-grants-1988_09