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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894361Generated: October 25, 2026

Sodium methanethiolate → tert-Butyl 4-((methylthio)methyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/1894361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium methanethiolateHCID 4378561—
Reactant1-(tert-Butoxycarbonyl)-4-((p-toluenesulfonyloxy)methyl)piperidineHCID 10642851—
SolventMethanolHCID 887—
Producttert-Butyl 4-((methylthio)methyl)piperidine-1-carboxylateHCID 2108727698.2%

Reaction Steps

To a solution of 4-(toluene-4-sulfonyloxymethyl)-piperidine-1-carboxylic acid tert-butyl ester (9.765 g, 26.43 mmol) in methanol (1 00mL) at room temperature was added sodium thiomethoxide (5.557 g, 79.29 mmol, Aldrich). The reaction mixture was stirred at room temperature for 2 h then concentrated. The residue was taken in methylene chloride and washed with water (3×) and brine (1×). The organic layer was dried over anhydrous sodium sulfate and concentrated to give a clear oil as crude product of 4-methylsulfanylmethyl-piperidine-1-carboxylic acid tert-butyl ester (6.37 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513239B2
Source datasetuspto-grants-2013_08
ORD IDord-417ca69b37364c94ae112a5df2ac1c7c
Source noteuspto-grants-2013_08