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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2401099Generated: October 30, 2026

Water → BOC-4-((S)-2-Methyl-pyrrolidin-1-yl)piperidine

https://huagongshe.com/reaction/2401099

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant(2S)-2-methylpyrrolidineHCID 6999702—
Reactant1-(tert-Butoxycarbonyl)-4-(p-toluenesulfonyloxy)piperidineHCID 15734713—
SolventAcetonitrileHCID 6342—
ProductBOC-4-((S)-2-Methyl-pyrrolidin-1-yl)piperidineHCID 5846806440%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 4-(toluene-4-sulfonyloxy)-piperidine-1-carboxylic acid tert-butyl ester (8.1 g, 22.8 mmol), (S)-(+)-2-methylpyrrolidine (2.33 g, 27.36 mmol), K2CO3 (6.93 g, 50.16 mmol) in acetonitrile (76 mL) was heated to 80° C. for 20 h and then added additional (S)-(+)-2-methylpyrrolidine (834 mg, 9.79 mmol), and the temperature of the reaction mixture was maintained at 80° C. for 20 h. The heating was removed and the solution was concentrated to provide a residue which was taken up with H2O (100 mL) and extracted with CH2Cl2 (2×100 mL). The organic layers were dried over K2CO3, filtered and concentrated to provide a crude oil which was purified by flash column chromatography (0 to 5% MeOH/CH2Cl2) to provide 2.43 g (40% yield) of the title compound as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796278B2
Source datasetuspto-grants-2014_08
ORD IDord-5712522f406e44f0a0c94d3bc967db34
Source noteuspto-grants-2014_08