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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 5092Generated: October 25, 2026

Sodium Chloride → 4-(4-Methoxybenzylthio)-1-methylpiperidine

https://huagongshe.com/reaction/5092

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ChlorideHCID 5234—
ReactantSodium hydrideHCID 24758—
Reactant4-Methoxy-alpha-toluenethiolHCID 80407—
Reactant1-Methylpiperidin-4-yl methanesulfonateHCID 4190681—
SolventDimethylformamideHCID 6228—
Product4-(4-Methoxybenzylthio)-1-methylpiperidineHCID 19797259—

Reaction Steps

10.9 ml of 4-methoxybenzyl mercaptan were dissolved in 55 ml of dry dimethylformamide, and 3.4 g of sodium hydride (as a 55% w/w suspension in mineral oil) were added to the solution, whilst ice-cooling. The mixture was then stirred at room temperature for 30 minutes. At the end of this time, a solution of 12.6 g of 4-methanesulfonyloxy-1-methylpiperidine in 63 ml of dry dimethylformamide was added to the mixture, which was then allowed to stand overnight at room temperature. The reaction mixture was then poured into an aqueous solution of sodium chloride and extracted with ethyl acetate. The extract as washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was purified by column chromatography through silica gel (eluted with a 1:4 by volume mixture of ethyl acetate and methanol) to afford 9.01 g of the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05242914
Source datasetuspto-grants-1993_09
ORD IDord-f4333880ec444bb9b8b94a7c224f7aa8
Source noteuspto-grants-1993_09