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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220208Generated: October 30, 2026

Potassium Carbonate → tert-Butyl (1-cyclopentylpiperidin-4-yl)carbamate

https://huagongshe.com/reaction/220208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantIodocyclopentaneHCID 73784—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
SolventAcetonitrileHCID 6342—
Producttert-Butyl (1-cyclopentylpiperidin-4-yl)carbamateHCID 53255879—

Reaction Steps

This compound was synthesized from the commercially available piperidin-4-yl-carbamic acid tert-butyl ester (2) (5 g, 25 mmol, 1 equiv) which was dissolved in acetonitrile (150 mL), followed by the addition of iodo-cyclopentane (9.79 g, 50 mmol, 2 equiv) and K2CO3 (3.45 g, 25 mmol, 1 equiv). The solution was stirred at room temperature for 48 hours. Due to the incompleteness of the reaction, iodocyclo-pentane (1.70 g, 8.69 mmol, 0.35 equiv) and K2CO3 (1 g, 7.25 mmol, 0.29 equiv) were added to the solution. The solution was stirred at room temperature for several hours. The solution was filtered over a bed of dicalite and the filtrate was evaporated under reduced pressure to obtain 3 (6.70 g, 25 mmol, quantitative). LRMS (ES+): m/z 269.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202887B2
Source datasetuspto-grants-2012_06
ORD IDord-9c998cb6ea894466b8b45319bb1fbd67
Source noteuspto-grants-2012_06