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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555367Generated: October 30, 2026

tert-Butanol → 1-Benzyl-4-(N-Boc-amino)piperidine

https://huagongshe.com/reaction/555367

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-ButanolHCID 6386—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
ReactantTert-butyldicarbonateHCID 22064466—
SolventSodium HydroxideHCID 14798—
Product1-Benzyl-4-(N-Boc-amino)piperidineHCID 443861882.8%

Reaction Steps

1-Benzylpiperidin-4-ylamine (3 g, 15.8 mmol) as a starting material was dissolved in 1M aqueous sodium hydroxide solution (35.8 ml) and t-butanol (32 ml) in a 250 ml vessel, and t-butyl-dicarbonate ((t-Boc)2O; 3.79 g, 17.38 mmol) was added thereto while stirring. The resulting mixture was reacted at room temperature for 12 hrs. After the completion of reaction, the reaction mixture was extracted with ethyl acetate twice. The organic layer was separated, washed with 0.1N hydrochloric acid aqueous solution and brine in order, dried over anhydrous sodium sulfate, filtered, and concentrated under reduced pressure. The residue thus obtained was subjected to a silica gel column chromatography to obtain 3.801 g of the title compound as a white solid (82.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08053435B2
Source datasetuspto-grants-2011_11
ORD IDord-cca69a15a3da469588d354684113ea3a
Source noteuspto-grants-2011_11