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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 555346Generated: October 29, 2026

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

https://huagongshe.com/reaction/555346

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), the 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, and 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. Then, the organic layer was washed with 0.1N hydrochloric acid solution and brine in order, dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue thus obtained was purified with a silica gel column chromatography to obtain 3.80 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-1bc73f53efec4300b220744484a65aea
Source noteuspto-grants-2011_11