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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192612Generated: November 2, 2026

Cyclobutanone → Tert-butyl 4-cyclobutylpiperazine-1-carboxylate

https://huagongshe.com/reaction/1192612

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanoneHCID 14496—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-cyclobutylpiperazine-1-carboxylateHCID 57423951—

Reaction Steps

To a mixture of tert-butyl piperazine-1-carboxylate (0.72 g, 0.0039 mol) and cyclobutanone (0.87 mL, 0.012 mol) in acetonitrile (10 mL) and tetrahydrofuran (10 mL) was added sodium triacetoxyborohydride (2.4 g, 0.012 mol). The resulting mixture was stirred at room temperature for 4 hours. The reaction was quenched with aq. NaHCO3 solution and extracted with dichloromethane. The combined organic layers were dried over MgSO4 and concentrated to give tert-butyl 4-cyclobutylpiperazine-1-carboxylate, which was treated with 4.57 M hydrogen chloride in 1,4-dioxane (10 mL, 0.04 mol) at room temperature for 2 hours and then evaporated to dryness to give the desired product. LCMS calculated for C8H17N2 (M+H)+: m/z=141.1; Found: 141.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-6b6c680f8d6146c986de4ae8fafc2195
Source noteuspto-grants-2014_03