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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 603161Generated: October 30, 2026

Benzyl 4-[((3R)-1-{3-[4-(methylsulfonyl)phenyl]propyl}piperidin-3-yl)methyl]piperazine-1-carboxylate → 1-[((3R)-{3-[4-(methylsulfonyl)phenyl]propyl}piperidin-3-yl)methyl]piperazine

https://huagongshe.com/reaction/603161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-[((3R)-1-{3-[4-(methylsulfonyl)phenyl]propyl}piperidin-3-yl)methyl]piperazine-1-carboxylateHCID 57656816—
SolventMethanolHCID 887—
Product1-[((3R)-{3-[4-(methylsulfonyl)phenyl]propyl}piperidin-3-yl)methyl]piperazineHCID 5765673495.1%

Reaction Steps

Benzyl 4-[((3R)-1-{3-[4-(methylsulfonyl)phenyl]propyl}piperidin-3-yl)methyl]piperazine-1-carboxylate (5.00 g, 9.70 mmol) was dissolved in methanol (30 ml) in a three-necked flask. The air was removed under reduced pressure and replaced with argon before the addition of 10% Pd/C (1.00 g). A balloon of hydrogen was then added and the reaction stirred at room temperature for 18 h. The hydrogen was evacuated and replaced with argon. The catalyst was then filtered using a nylon whatman autocup and the solvent removed under reduced pressure to afford the desired product as a yellow gum (3.50 g, 95% crude yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07906645B2
Source datasetuspto-grants-2011_03
ORD IDord-299b01b9338e4e079506883cfa7aea72
Source noteuspto-grants-2011_03